Anmelden

Reducing Agents

Überblick

Source: Vy M. Dong and Daniel Kim, Department of Chemistry, University of California, Irvine, CA

Controlling the reactivity and selectivity during the synthesis of a molecule is very important criteria for chemists. This has led to the development of many reagents that allow chemists to pick and choose reagents suitable for a given task. Quite often, a balance between reactivity and selectivity needs to be achieved. This experiment will use IR spectroscopy to monitor the reaction and to understand the reactivity of carbonyl compounds as well as the reactivity of hydride-reducing reagents.

Verfahren

1. Measuring Properties of Ethyl Acetoacetate

  1. Take an IR of the starting material (ethyl acetoacetate).
  2. Take a TLC using 40% ethyl acetate in 60% hexanes.

2. Reduction of Ethyl Acetoacetate with Sodium Borohydride

  1. Add 1 mmol of ethyl acetoacetate to a round-bottom flask.
  2. Add 5 mL of ethanol and swirl to mix completely.
  3. Lower the beaker into an ice-water bath.
  4. Weigh 1 mmol of sodium borohydride and slowly add to the stirred

Log in or to access full content. Learn more about your institution’s access to JoVE content here

Ergebnisse

Figure 1
Figure 1. Representative IR results for ethyl 3-hydroxybutyrate.

Log in or to access full content. Learn more about your institution’s access to JoVE content here

Anwendung und Zusammenfassung

The trends of carbonyl reactivity and hydride donor ability have been reviewed and demonstrated. The visual reactiveness of the two commonly used reagents is apparent and can be appreciated.

The understanding of the reactivity of reagents and functional groups is of high importance when developing new methods for reductions or any other kind of reaction. Controlling the selectivity and reactivity of any reaction is an important factor to consider when deciding on the reagents used for a chemic

Log in or to access full content. Learn more about your institution’s access to JoVE content here

Tags
Reducing AgentsCarbonylsOrganic ChemistryReactantsReduction ProductsChemical CompositionElectrophilicNucleophilic AttackHydride TransferAcyl HalidesKetonesAldehydesEstersAmidesCarboxylic Acids

pringen zu...

0:04

Overview

1:00

Principles of Carbonyl Reduction

3:37

Reducing Ethyl Acetoacetate with Sodium Borohydride

5:34

Reducing Ethyl Acetoacetate with Lithium Aluminum Hydride

7:20

Results

8:36

Applications

9:58

Summary

Videos aus dieser Sammlung:

article

Now Playing

Reducing Agents

Organic Chemistry II

42.7K Ansichten

article

Cleaning Glassware

Organic Chemistry II

123.1K Ansichten

article

Nucleophilic Substitution

Organic Chemistry II

99.2K Ansichten

article

Grignard Reaction

Organic Chemistry II

148.7K Ansichten

article

n-Butyllithium Titration

Organic Chemistry II

47.6K Ansichten

article

Dean-Stark Trap

Organic Chemistry II

99.7K Ansichten

article

Ozonolysis of Alkenes

Organic Chemistry II

66.7K Ansichten

article

Organocatalysis

Organic Chemistry II

16.6K Ansichten

article

Palladium-Catalyzed Cross Coupling

Organic Chemistry II

34.2K Ansichten

article

Solid Phase Synthesis

Organic Chemistry II

40.8K Ansichten

article

Hydrogenation

Organic Chemistry II

49.1K Ansichten

article

Polymerization

Organic Chemistry II

93.6K Ansichten

article

Melting Point

Organic Chemistry II

149.6K Ansichten

article

Infrared Spectroscopy

Organic Chemistry II

213.8K Ansichten

article

Polarimeter

Organic Chemistry II

99.8K Ansichten

JoVE Logo

Datenschutz

Nutzungsbedingungen

Richtlinien

Forschung

Lehre

ÜBER JoVE

Copyright © 2025 MyJoVE Corporation. Alle Rechte vorbehalten