Organocatalysis

Panoramica

Source: Vy M. Dong and Faben Cruz, Department of Chemistry, University of California, Irvine, CA

This experiment will demonstrate the concept of organocatalysis by illustrating the proper setup of a reaction that utilizes enamine catalysis. Organocatalysis is a form of catalysis that uses substoichiometric amounts of small organic molecules to accelerate reactions. This type of catalysis is complementary to other forms of catalysis such as transition metal or biocatalysis. Transition metal catalysis involves transition metals as catalysts and biocatalysis uses enzymes as catalysts. Some advantages of organocatalysis include the low toxicity and cost of the organocatalysts in comparison to many metal catalysts. In addition, most organocatalysts are not sensitive to air and moisture, unlike metal catalysts. In contrast to enzymes found in living organisms, the small molecules that act as organocatalysts are typically easy to access. Furthermore, organocatalysis offers complementary and new reactivity not observed with other forms of catalysis.

Procedura

Figure 2

  1. Add (S)-proline (40 mg, 0.35 mmol, 0.35 equivalents), acetonitrile (MeCN, 5 mL), and the diketone (126 mg, 1 mmol, 1 equivalent) to a round-bottom flask (~ 20 mL) equipped with a magnetic stir bar.
  2. Stir the reaction mixture at 35 °C for 30 min.
  3. Add 3-buten-2-one (105 mg, 1.5 mmol, 1.5 equivalents) dropwise at 35 °C and stir at the same temperature for 1 week.
  4. Cool the reaction to room temperat

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Risultati

The purified product should have the following 1H NMR spectrum: 1H NMR δ 5.88 (1H, s), 2.6-2.7 (2H, m), 2.3-2.55 (4H, m), 2.0-2.2 (2H, m), 1.6-1.8 (2H, m), 1.4 (3H, s).

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Tags
OrganocatalysisOrganocatalystsTransition MetalsEnzymesLow CostLow ToxicitySynthesizedObtainedSmall Organic MoleculesAccelerate ReactionsEnamine Catalyzed ReactionApplications Of OrganocatalysisCovalent InteractionsReactive IntermediateActivationLewis BasesElectron DonorsVersatilityNucleophilicityAlkylationAldol ReactionsIminium CatalystsElectrophilicityMichael AdditionsCycloadditionsStereoisomer ProductsAsymmetric CatalysisProline Catalysis

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0:04

Overview

0:44

Principles of Organocatalysis

2:34

Organocatalytic Aldol Reaction

4:03

Results

4:48

Applications

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Summary

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