Catalytic hypervalent iodine oxidation of alcohols to the corresponding carbonyl compounds usingN-hydroxyphthalimide (NHPI) andm-chloroperbenzoic acid

Author:

Zhu Chenjie1,Ji Lei1,Zhang Qian1,Wei Yunyang1

Affiliation:

1. School of Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.

Abstract

An efficient, facile, and mild oxidation of alcohols to the corresponding carbonyl compounds with m-chloroperbenzoic acid (mCPBA) and N-hydroxyphthalimide (NHPI) in the presence of a catalytic amount of iodobenzene was reported. The oxidation proceeded in mixed solvent at room temperature to afford carbonyl compounds in excellent yields. A possible mechanism for the oxidation was proposed.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Reference54 articles.

1. (a) Tojo, G.; Fernández, M.Oxidation of Primary Alcohols to Carboxylic Acids;Springer: Berlin, 2006;

2. (b) Tojo, G.; Fernández, M.Oxidation of Alcohols to Aldehydes and Ketones;Springer: Berlin, 2006;

3. Large-Scale Oxidations in the Pharmaceutical Industry

4. (a) Varvoglis, A.Hypervalent Iodine in Organic Chemistry;Academic Press: London, 1997;

5. Organic Polyvalent Iodine Compounds

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