Silica Sulfuric Acid as a Reusable Catalyst for the Conversion of Ketones into Amides by a Schmidt Reaction under Solvent-Free Conditions

Author:

Eshghi Hossein12,Hassankhani Asadollah2,Mosaddegh Elaheh2

Affiliation:

1. Department of Chemistry, Ferdowsi University of Mashhad, Mashhad 91775-1436, Iran

2. Department of Chemistry, Sistan and Baluchestan University Zahedan 98135-674 Iran

Abstract

Silica sulfuric acid is a highly efficient reagent for the conversion of a variety of ketones into the corresponding amides by a Schmidt reaction under solvent-free conditions. Cyclic, aliphatic and aromatic ketones with electron-donating or withdrawing substituents may be converted easily in excellent yield. The major advantages of this method are: operational simplicity, the ready availability of the reagent, selectivity, general applicability, mild reaction conditions, short reaction times and high yields. The recovered catalyst could be used in new attempts without any purification.

Publisher

SAGE Publications

Subject

General Chemistry

Reference30 articles.

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2. Nitrogen insertion reactions of bridged bicyclic ketones. Regioselective lactam formation

3. The Schmidt Reaction of Some p-Substituted Acetophenones

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