Name: employing pressurized hot water extraction (phwe) to explore natural products chemistry in the undergraduate laboratory
Uploaded: 2018-11-07T13:00:00
Description: Watch this Scientific Journal Video about Employing Pressurized Hot Water Extraction PHWE to Explore Natural Products Chemistry in the Undergraduate Laboratory at JoVE.com

The authors acknowledge the School of Natural Sciences - Chemistry, University of Tasmania and the School of Chemistry, The University of Sydney for financial support. B.J.D. and J.J. thank the Australian Government for Research Training Program Scholarships.

NOTE: It is advisable that all procedures are performed in a fume hood. Students must wear appropriate personal protective equipment at all times in the laboratory and the safety data sheets (SDS) associated with each reagent must be consulted before use.
1. PHWE of cloves: isolation of eugenol and acetyleugenol
<ol>
	<li>Extraction of eugenol and acetyleugenol from cloves
	<ol>
		<li>Place coarsely ground cloves (12.5 g) in a 250-mL beaker.</li>
		<li>Add s...

<ol>
	<li>Newman, D. J., Cragg, G. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Natural+Products+as+Sources+of+New+Drugs+from+1981+to+2014.">Natural Products as Sources of New Drugs from 1981 to 2014.</a> Journal of Natural Products. 79, 629-661 (2016).</li><li>Barnes, E. C., Kumar, R., Davis, R. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+use+of+isolated+natural+products+as+scaffolds+for+the+generation+of+chemically+diverse+screening+libraries+for+drug+discovery.">The use of isolated natural products as scaffolds for the generation of chemically diverse screening libraries for drug discovery.</a> Natural Product Reports. 33, 372-381 (2016).</li><li>DeCorte, B. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Underexplored+Opportunities+for+Natural+Products+in+Drug+Discovery.">Underexplored Opportunities for Natural Products in Drug Discovery.</a> Journal of Medicinal Chemistry. 59, 9295-9304 (2016).</li><li>Bucar, F., Wube, A., Schmid, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Natural+product+isolation+-+how+to+get+from+biological+material+to+pure+compounds.">Natural product isolation - how to get from biological material to pure compounds.</a> Natural Product Reports. 30, 525-545 (2013).</li><li>Sticher, O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Natural+product+isolation.">Natural product isolation.</a> Natural Product Reports. 25, 517-554 (2008).</li><li>Just, J., Deans, B. J., Olivier, W. J., Paull, B., Bissember, A. C., Smith, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=New+Method+for+the+Rapid+Extraction+of+Natural+Products:+Efficient+Isolation+of+Shikimic+Acid+from+Star+Anise.">New Method for the Rapid Extraction of Natural Products: Efficient Isolation of Shikimic Acid from Star Anise.</a> Organic Letters. 17, 2428-2430 (2015).</li><li>Caprioli, G., Cortese, M., Cristalli, G., Maggi, F., Odello, L., Ricciutelli, M., Sagratini, G., Sirocchi, V., Tomassoni, G., Vittori, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Optimization+of+espresso+machine+parameters+through+the+analysis+of+coffee+odorants+by+HS-SPME-GC/MS.">Optimization of espresso machine parameters through the analysis of coffee odorants by HS-SPME-GC/MS.</a> Food Chemistry. 135, 1127-1133 (2012).</li><li>Just, J., Jordan, T. B., Paull, B., Bissember, A. C., Smith, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Practical+isolation+of+polygodial+from+Tasmannia+lanceolata:+a+viable+scaffold+for+synthesis.">Practical isolation of polygodial from Tasmannia lanceolata: a viable scaffold for synthesis.</a> Organic Biomolecular Chemistry. 13, 11200-11207 (2015).</li><li>Just, J., Bunton, G. L., Deans, B. J., Murray, N. L., Bissember, A. C., Smith, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Extraction+of+Eugenol+from+Cloves+Using+an+Unmodified+Household+Espresso+Machine:+An+Alternative+to+Traditional+Steam+Distillation.">Extraction of Eugenol from Cloves Using an Unmodified Household Espresso Machine: An Alternative to Traditional Steam Distillation.</a> Journal of Chemical Education. 93, 213-216 (2016).</li><li>Deans, B. J., Bissember, A. C., Smith, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Practical+Isolation+of+Asperuloside+from+Coprosma+quadrifida+via+Rapid+Pressurised+Hot+Water+Extraction.">Practical Isolation of Asperuloside from Coprosma quadrifida via Rapid Pressurised Hot Water Extraction.</a> Australian Journal of Chemistry. 69, 1219-1222 (2016).</li><li>Deans, B. J., Just, J., Chetri, J., Burt, L. K., Smith, J. N., Kilah, N. L., de Salas, M., Gueven, N., Bissember, A. C., Smith, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Pressurized+Hot+Water+Extraction+as+a+Viable+Bioprospecting+Tool:+Isolation+of+Coumarin+Natural+Products+from+Previously+Unexamined+Correa+(Rutaceae).">Pressurized Hot Water Extraction as a Viable Bioprospecting Tool: Isolation of Coumarin Natural Products from Previously Unexamined Correa (Rutaceae).</a> ChemistrySelect. 2, 2439-2443 (2017).</li><li>Deans, B. J., Olivier, W. J., Girbino, D., Bissember, A. C., Smith, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Extraction+of+carboxylic+acid-containing+diterpenoids+from+Dodonaea+viscosa+via+pressurised+hot+water+extraction.">Extraction of carboxylic acid-containing diterpenoids from Dodonaea viscosa via pressurised hot water extraction.</a> Fitoterapia. 126, 65-68 (2018).</li><li>Deans, B. J., Kilah, N. L., Jordan, G. J., Bissember, A. C., Smith, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Arbutin+Derivatives+Isolated+from+Ancient+Proteaceae:+Potential+Phytochemical+Markers+Present+in+Bellendena,+Cenarrhenes+and+Persoonia+Genera.">Arbutin Derivatives Isolated from Ancient Proteaceae: Potential Phytochemical Markers Present in Bellendena, Cenarrhenes and Persoonia Genera.</a> Journal of Natural Products. 81, 1241-1251 (2018).</li><li>Deans, B. J., Tedone, L., Bissember, A. C., Smith, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Phytochemical+profile+of+the+rare,+ancient+clone+Lomatia+tasmanica+and+comparison+to+other+endemic+Tasmanian+species+L.+tinctoria+and+L.+polymorpha.">Phytochemical profile of the rare, ancient clone Lomatia tasmanica and comparison to other endemic Tasmanian species L. tinctoria and L. polymorpha.</a> Phytochemistry. 153, 74-78 (2018).</li><li>Deans, B. J., Skierka, B., Karagiannakis, B. W., Vuong, D., Lacey, E., Smith, J. A., Bissember, A. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Siliquapyranone:+a+Tannic+Acid+Tetrahydropyran-2-one+Isolated+from+the+Leaves+of+Carob+(Ceratonia+siliqua)+by+Pressurised+Hot+Water+Extraction.">Siliquapyranone: a Tannic Acid Tetrahydropyran-2-one Isolated from the Leaves of Carob (Ceratonia siliqua) by Pressurised Hot Water Extraction.</a> Australian Journal of Chemistry. 71, (2018).</li><li>Olivier, W. J., Kilah, N. L., Horne, J., Bissember, A. C., Smith, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=ent-Labdane+Diterpenoids+from+Dodonaea+viscosa.">ent-Labdane Diterpenoids from Dodonaea viscosa.</a> Journal of Natural Products. 79, 3117-3126 (2016).</li><li>Rihak, K. J., Bissember, A. C., Smith, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Polygodial:+A+viable+natural+product+scaffold+for+the+rapid+synthesis+of+novel+polycyclic+pyrrole+and+pyrrolidine+derivatives.">Polygodial: A viable natural product scaffold for the rapid synthesis of novel polycyclic pyrrole and pyrrolidine derivatives.</a> Tetrahedron. 74, 1167-1174 (2018).</li><li>Ntamila, M. S., Hassanali, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Isolation+of+Oil+of+Clove+and+Separation+of+Eugenol+and+Acetyl+Eugenol.">Isolation of Oil of Clove and Separation of Eugenol and Acetyl Eugenol.</a> Journal of Chemical Education. 53, 263 (1976).</li><li>Still, W. C., Kahn, M., Mitra, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Rapid+chromatographic+technique+for+preparative+separations+with+moderate+resolution.">Rapid chromatographic technique for preparative separations with moderate resolution.</a> Journal of Organic Chemistry. , 2923-2925 (1978).</li></ol>

The classical procedure for isolating eugenol from cloves by steam distillation has been part of the intermediate chemistry laboratory program at the University of Sydney for decades but was modernized to employ PHWE methodology in 2016 (Figure 1).9,18 This provided a number benefits. Firstly, utilizing household espresso machines in the laboratory environment immediately fascinated and engaged students by illustrating the applicatio...

The isolation and identification of natural products are of fundamental importance to the scientific community and society more generally.1 Bioprospecting, the search for valuable organic molecules found in nature,remains an indispensable process in the discovery of new drug leads and potential therapeutic agents. It is estimated that, from 1981-2014, ~75% of all approved small molecule pharmaceutical drugs were natural products, natural product-derived or natural product-inspired.1 Furthermore, natural products possess enormous structural and chemical diversity. For this reason, they also represent valuable chemical scaffolds that can be directly used in organic synthesis or in the development of chiral ligands and catalysts.2,3
Traditionally, relatively time-intensive procedures such as maceration, Soxhlet extraction, and steam distillation have been the mainstay of research focused on the isolation of secondary metabolites from plants.4 More modern extraction techniques, including accelerated solvent extraction, have focused on reducing extraction times and establishing greener protocols.4,5 In 2015, an original pressurized hot water extraction (PHWE) method was reported.6 This technique employed an unmodified household espresso machine to facilitate the rapid and particularly efficient extraction of shikimic acid from star anise. Espresso machines have been specifically designed and engineered to extract organic molecules from appropriately ground coffee beans. To achieve this, these instruments heat water at temperatures up to 96 &#176;C and at pressures of typically 9 bar.7 With this in mind, it is perhaps not surprising that espresso machines can be utilized to efficiently extract natural products from a range of plant material.
Subsequent studies involving a variety of terrestrial plant species have demonstrated the capacity of this PHWE technique to efficiently extract natural products across a relatively broad polarity range.6,8,9,10,11,12,13,14,15 Furthermore, compounds containing somewhat sensitive functional groups, such as aldehydes, epoxides, glycosides, and potentially epimerizable stereogenic centers were typically unaffected by the extraction process. The complementary nature of this technique relative to more traditional methods has also been demonstrated.12,16 This PHWE method has also been employed to isolate multi-gram quantities of natural products, which have been used to prepare novel natural product derivatives and in complex molecule synthesis more generally.8,11,17
It was identified that this new PHWE method could serve as a useful teaching tool that could be incorporated in the undergraduate laboratory. This primarily derives from the rapid nature of this technique relative to the traditional extraction methods that are often incompatible with the time constraints associated with undergraduate laboratory experiments. Consequently, this technique supplanted the traditional undergraduate chemistry laboratory experiment focused on the extraction of eugenol from cloves employing steam-distillation at the University of Tasmania.9,18 Since that time, variations of this experiment have been adopted by other universities and a modified experiment focusing on the PHWE of cloves now features in the undergraduate chemistry laboratory program at the University of Sydney (vide infra).
In order to demonstrate the practicality and feasibility of employing this new PHWE approach for teaching purposes, two protocols are presented as part of this study. The first part of this report highlights an experiment on the PHWE of eugenol and acetyleugenol from cloves which is part of the second-year undergraduate laboratory program at the University of Sydney (Figure 1). This experiment serves to introduce students to natural products chemistry while developing fundamental practical skills. The second part features an experiment on the PHWE of the endemic Australian plant species Correa reflexa which is part of the third-year undergraduate laboratory program at the University of Tasmania (Figure 2). This experiment is designed to simulate natural products bioprospecting and reinforce core laboratory techniques.11

<table border="0" cellpadding="0" cellspacing="0" style="width:1069px;" width="1070">
	<tbody>
		<tr height="40">
			<td height="40" style="height:40px;width:216px;">espresso machines</td>
			<td style="width:167px;">Breville/Sunbeam</td>
			<td style="width:520px;">Breville espresso machine model 800ES / Sunbeam EM3820 Caf&#233; Espresso II</td>
			<td style="width:167px;"></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;width:216px;">rotary evporators</td>
			<td style="width:167px;">Buchi and Heidolph</td>
			<td style="width:520px;"></td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">cloves (plant material)</td>
			<td>Dijon Food Pty Ltd</td>
			<td></td>
			<td>Cloves must be ground in a food processor for students.</td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">Correa reflexa (plant material)</td>
			<td>sample obtained in Tasmania</td>
			<td>Sample collected from mature shrubs in the Thomas Crawford Reserve at the University of Tasmania</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;width:216px;">sand</td>
			<td style="width:167px;">Ajax</td>
			<td style="width:520px;">1199</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">ethanol</td>
			<td>Redoc Chemicals</td>
			<td>E95 F3</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">hexanes</td>
			<td>Ajax</td>
			<td>251</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">magnesium sulfate</td>
			<td>Ajax</td>
			<td>1548</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">diethyl ether</td>
			<td>Merck</td>
			<td>1009215000</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">silica on aluminium TLC plates</td>
			<td>Merck</td>
			<td>1055540001</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">eugenol</td>
			<td>Merck</td>
			<td>1069620100</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">eugenyl acetate</td>
			<td>Aldrich</td>
			<td>W246905</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">acetone</td>
			<td>Redox Chemicals</td>
			<td>Aceton13</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">cyclohexane</td>
			<td>ChemSupply</td>
			<td>CA019</td>
			<td></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;">silica gel 60</td>
			<td>Trajan</td>
			<td>5134312</td>
			<td style="width:167px;">40 - 63um (230-400mesh)</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Congo red paper</td>
			<td>ChemSupply</td>
			<td>IS070-100S</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">32% hydrochloric acid</td>
			<td>Ajax</td>
			<td>256</td>
			<td></td>
		</tr>
	</tbody>
</table>

employing pressurized hot water extraction (phwe) to explore natural products chemistry in the undergraduate laboratory

A recently developed pressurized hot water extraction (PHWE) method which utilizes an unmodified household espresso machine to facilitate natural products research has also found applications as an effective teaching tool. Specifically, this technique has been used to introduce second- and third-year undergraduates to aspects of natural products chemistry in the laboratory. In this report, two experiments are presented: the PHWE of eugenol and acetyleugenol from cloves and the PHWE of seselin and (+)-epoxysuberosin from the endemic Australian plant species Correa reflexa. By employing PHWE in these experiments, the crude clove extract, enriched in eugenol and acetyleugenol, was obtained in 4-9% w/w from cloves by second-year undergraduates and seselin and (+)-epoxysuberosin were isolated in yields of up to 1.1% w/w and 0.9% w/w from C. reflexa by third-year students. The former exercise was developed as a replacement for the traditional steam distillation experiment providing an introduction to extraction and separation techniques, while the latter activity featured guided-inquiry teaching methods in an effort to simulate natural products bioprospecting. This primarily derives from the rapid nature of this PHWE technique relative to traditional extraction methods that are often incompatible with the time constraints associated with undergraduate laboratory experiments. This rapid and practical PHWE method can be used to efficiently isolate various classes of organic molecules from a range of plant species. The complementary nature of this technique relative to more traditional methods has also been demonstrated previously.

PHWE of cloves. When attempting to perform the liquid-liquid extraction step, students often encountered emulsions (the addition of brine was typically not effective). At this stage, students were instructed to allow the mixture to stand in the separating funnel while they explored the effects of eluent composition on the separation of eugenol and acetyleugenol by TLC. It should be noted that hexane can be substituted with either heptane or dichloromethane in the liquid-liquid extraction ...

Watch this Scientific Journal Video about Employing Pressurized Hot Water Extraction PHWE to Explore Natural Products Chemistry in the Undergraduate Laboratory at JoVE.com

Employing Pressurized Hot Water Extraction PHWE to Explore Natural Products Chemistry in the Undergraduate Laboratory

Here, we employ a pressurized hot water extraction (PHWE) method, which utilizes an unmodified household espresso machine to introduce undergraduates to natural products chemistry in the laboratory. Two experiments are presented: PHWE of eugenol and acetyleugenol from cloves and PHWE of seselin and (+)-epoxysuberosin from the Australian plant Correa reflexa.

Employing Pressurized Hot Water Extraction (PHWE) to Explore Natural Products Chemistry in the Undergraduate Laboratory

A recently developed pressurized hot water extraction (PHWE) method which utilizes an unmodified household espresso machine to facilitate natural products ...

This technique represents an inherently practical and efficient strategy for natural products extraction in isolation chemistry. And we think it's a useful and complimentary extraction tool. Because this is a rapid flow process, the extract is only heated for a short period and the extraction of intractable plant pigments which often complicate purification is minimized.We think that this technique is well suited to enabling chemo taxonomic sampling in addition to medicinal chemistry by facilitating bio prospecting which is the search for valuable molecules in nature. Visual demonstration of this method is important as a sample preparation in extraction steps are most effectively explained visually. This also reinforces the simplicity of the extraction and its appropriate use in the undergraduate laboratory environment.Place 12.5 grams of coarsely ground cloves into a 250 milliliter beaker. Add 12.5 grams of sand and mix well. Next, collect a portafilter and load the basket with the entire clove and sand mixture.Use a tamper to lightly compress the sample making sure not to compress it too much which would prevent fluid from flowing. Load the portafilter into the espresso machine and place a clear 250 milliliter beaker beneath it. Add a solution containing 30 percent ethanol in water to the water tank.Using the espresso machine, collect 100 milliliters of the extract. Let the portafilter finish dripping and then remove it from the espresso machine. Use a spatula to remove the clove grinds from the portafilter and discard them into a solid waste container.Rinse out any residual solids with tap water in the sink. Transfer the beaker containing the clove extracts to an ice bath and let it cool until the temperature reduced to at least 30 degrees celsius. In a fume hood, pour the cooled extract into a 250 milliliter separatory funnel.Add 30 milliliters of hexane and mix by shaking gently. Place the separatory funnel in a ring clamp that is fitted to a retort stand and allow the aqueous and organic layers to separate. It can take up to 10 minutes for the layers to separate so we recommend that you carry out solvent optimization of TLCs while you wait.Collect the aqueous layer back into the 250 milliliter beaker. Transfer the organic layer which contains the product to a clean 250 milliliter conical flask. Then pour the aqueous face pack into the separatory funnel.Extract the aqueous layer two additional times with hexane. Using 30 milliliters of hexane each time. Combine the organic layers into the same 250 milliliter conical flask after each extraction.After the third liquid extraction pour the combined organic extract into the separatory funnel. Wash the organic extract by adding 100 milliliters of water and shaking vigorously. Collect the organic layer into a clean 250 milliliter conical flask.And then dry it by adding magnesium sulfate and swirling. Filter the dried mixture through fluted filter paper contained in a glass funnel into the round bottom flask. Using a rotary evaporator, evaporate the solvent from the collected filtrate.Then weigh the flask containing the resultant oil. Add 10 milliliters of hexane to the round bottom flask containing the crude eugenol containing extract. Pour the resulting solution into a 250 milliliter separatory funnel.Rinse the round bottom flask with 10 milliliters of hexane and add this to the separatory funnel. Extract the hexane solution twice with three molar aqueous sodium hydroxide via liquid liquid extraction. Using 25 milliliters of sodium hydroxide for each extraction.Collect the aqueous layers from each extraction and combine them in a 250 milliliter conical flask. Collect the organic layer in a 50 milliliter conical flask. Then dry it by adding magnesium sulfate to the flask and swirling it.Filter the solution through fluted filter paper contained in a glass funnel into a pre-weighed 100 milliliter round bottom flask. Discard the solid residue then use a rotary evaporator to remove the solvent. After this weigh the round bottom flask which now contains the resulting oil on a top pan balance.Next place the conical flask that contains the combined aqueous layers into an ice water bath. Swirl the flask while slowly adding a 10 molar solution of hydrochloric acid until a white emulsion is formed. Use a pipette to transfer a drop of this solution onto Congo red paper to test its acidity.The paper should turn blue. After this transfer the milky aqueous emulsion to a 250 milliliter separating flask. Make sure that the emulsion is at room temperature and then perform liquid liquid extraction twice using 30 milliliters of hexane per extraction.Combine the two hexane extracts into a clean 100 milliliter conical flask. Add magnesium sulfate to dry the solution. Filter the solution through fluted filter paper contained in a glass funnel into the pre-weighed 100 milliliter round bottom flask.Then use a rotary evaporator to remove the solvent. After this weigh the round bottom flask which now contains the resulting oil on a top pan balance. Using an electric spice grinder grind 10 grams of correa reflexa leaves for 20 to 30 seconds.Transfer the ground plant material to a 250 milliliter beaker. Add approximately two grams of coarse sand. Mix the sand and plant material together and then transfer it into the basket of a portafilter.Use a tamper to lightly compress the sample making sure not to compress it too much. Add about 300 milliliters of 35 percent ethanol in water to the espresso machine tank. Load the portafilter into the espresso machine and place a 250 milliliter beaker beneath it.Then collect approximately 100 milliliters of extract. Wait for about one minute then collect another 100 milliliters of extract. Transfer this mixture to an ice bath to cool.Use a rotary evaporator with a water bath temperature of 40 degrees celsius to evaporate the ethanol. Next transfer the aqueous extract to a seperatory funnel. Extract the solution twice with ethyl acetate using 50 milliliters of ethyl acetate per extraction.Combine the organic extracts. Add magnesium sulfate and swirl the flask to dry the solution. Then use a centered glass funnel to filter the solution and use a rotary evaporator to obtain the crude extract.In this procedure students are allocated a TLC solvent ratio of acetone and cyclohexane and provided with pure standards of eugenol and acetyl-eugenol. TLC analysis is performed and the effects of solvent composition on the retention factor are considered. The optimum solvent compositions are seen to typically range between five and 20 percent acetone cyclohexane.With a delta retention factor of 0.1 to 0.2. The different acid based properties of the two major organic molecules are then exploited to separate them by liquid liquid extraction. Typically eugenol was isolated in a yield of 45 to 65 percent of the crude extract while acetyl-eugenol was isolated in a yield of five to 10 percent.Students then utilized the optimized eluant to determine the success of their liquid liquid extraction by comparison of their extracts to the pure reference samples by TLC. Advanced students then subject half their isolated crude oil to flash column chromatography. While the complete separation of eugenol from acetyl-eugenol is rarely achieved due to their close retention factors, a few fractions containing pure eugenol are generally collected.Following this procedure, methods like nuclear magnetic resonance spectroscopy and gas chromatography mass spectrometry can be performed characterized the isolated compounds. Don't forget, working with hot liquids, relatively high pressures and corrosive liquids can be hazardous so precautions such as wearing personal protective equipment should be taken.

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A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products

The guanidine functional group, displayed most prominently in the amino acid arginine, one of the fundamental building blocks of life, is an important ...

In Situ Characterization of Hydrated Proteins in Water by SALVI and ToF-SIMS

In Situ Characterization of Hydrated Proteins in Water by SALVI and ToF-SIMS

This work demonstrates in situ characterization of protein biomolecules in the aqueous solution using the System for Analysis at the Liquid Vacuum ...

Synthesis of Protein Bioconjugates via Cysteine-maleimide Chemistry

Synthesis of Protein Bioconjugates via Cysteine-maleimide Chemistry

The chemical linking or bioconjugation of proteins to fluorescent dyes, drugs, polymers and other proteins has a broad range of applications, such as the ...

Laboratory Production of Biofuels and Biochemicals from a Rapeseed Oil through Catalytic Cracking Conversion

The work is based on a reported study which investigates the processability of canola oil (bio-feed) in the presence of bitumen-derived heavy gas oil ...

Synthesis of a Water-soluble Metal&#8211;Organic Complex Array

We demonstrate a method for the synthesis of a water-soluble multimetallic peptidic array containing a predetermined sequence of metal centers such as ...

Application and Methodology of the Non-destructive 19F Time-domain NMR Technique to Measure the Content in Fluorine-containing Drug Products

Application and Methodology of the Non-destructive 19F Time-domain NMR Technique to Measure the Content in Fluorine-containing Drug Products

Here, we describe a protocol developed by our group that uses low-field fluorine-19 (19F) time-domain (TD) nuclear magnetic resonance (NMR) to measure the ...

In Situ Characterization of Boehmite Particles in Water Using Liquid SEM

In Situ Characterization of Boehmite Particles in Water Using Liquid SEM

In situ imaging and elemental analysis of boehmite (AlOOH) particles in water is realized using the System for Analysis at the Liquid Vacuum Interface ...