Issue 12, 2016

Green and practical transition metal-free one-pot conversion of substituted benzoic acids to anilines using tosyl azide

Abstract

A simple one-pot procedure for conversion of 2-iodo/2-nitro benzoic acids and dihydropyranone fused benzoic acids into corresponding anilines, using tosyl azide, under transition metal-free conditions is explained. TsN3, is one of the more stable azides, much cheaper and easy to handle. This method is environmentally benign, adoptable for large scale preparation. Different factors such as steric and electronic effect of 2-iodo/2-nitro substituents, and the effect of conformational constraints of the fused dihydropyranone ring on co-planarity of the aromatic ring should contribute to the success of this reaction. Tosyl nitrene was found to be involved in the decarboxylation reaction. As this method is simple, scalable and requires only simple reagents we expect this method to find widespread application in organic synthesis.

Graphical abstract: Green and practical transition metal-free one-pot conversion of substituted benzoic acids to anilines using tosyl azide

Supplementary files

Article information

Article type
Research Article
Submitted
10 jul. 2016
Accepted
14 sep. 2016
First published
19 sep. 2016

Org. Chem. Front., 2016,3, 1680-1685

Green and practical transition metal-free one-pot conversion of substituted benzoic acids to anilines using tosyl azide

A. Ilangovan, P. Sakthivel and P. Sakthivel, Org. Chem. Front., 2016, 3, 1680 DOI: 10.1039/C6QO00343E

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