Issue 36, 2014

A novel oxidative procedure for the synthesis of benzamides from styrenes and amines under metal-free conditions

Abstract

An interesting procedure for the oxidative synthesis of amides from styrenes and amines has been developed. Various primary amides were formed in moderate yields (25–81%). Secondary amides can be produced in moderate yields as well (41–68%). Notably, no transition metal catalyst was needed for this transformation. This is the first example of oxidative transformation of styrenes to benzamides.

Graphical abstract: A novel oxidative procedure for the synthesis of benzamides from styrenes and amines under metal-free conditions

Supplementary files

Article information

Article type
Communication
Submitted
10 Feb 2014
Accepted
18 Mar 2014
First published
18 Mar 2014

Chem. Commun., 2014,50, 4747-4750

A novel oxidative procedure for the synthesis of benzamides from styrenes and amines under metal-free conditions

M. Sharif, J. Gong, P. Langer, M. Beller and X. Wu, Chem. Commun., 2014, 50, 4747 DOI: 10.1039/C4CC01054J

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