Issue 8, 2014

Unprecedented amidation of ‘transient’ aryl thioaldehydes by N,N-dimethylformamide under basic conditions

Abstract

An unprecedented reaction of N,N-dimethylformamide (DMF) with ‘transient’ aryl thiobenzaldehydes, derived from diaryl disulfides under basic conditions, is reported. The unique role of DMF has been generalized to construct a simple method for the synthesis of N,N-dimethyl aryl thioamides. A plausible mechanism for this transformation is discussed.

Graphical abstract: Unprecedented amidation of ‘transient’ aryl thioaldehydes by N,N-dimethylformamide under basic conditions

Supplementary files

Article information

Article type
Letter
Submitted
31 Mar 2014
Accepted
13 May 2014
First published
16 May 2014

New J. Chem., 2014,38, 3367-3370

Unprecedented amidation of ‘transient’ aryl thioaldehydes by N,N-dimethylformamide under basic conditions

B. Basu and S. Kundu, New J. Chem., 2014, 38, 3367 DOI: 10.1039/C4NJ00480A

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