Issue 60, 2014

Hypervalent iodine-catalyzed oxidative amidation of methylarenes

Abstract

Hypervalent iodine-catalyzed oxidative amidation of methylarenes to the corresponding amides by using an oxidant (tert-butyl hydroperoxide, 70% aqueous solution) is discussed. This oxidizing agent presented a high degree of selectivity for the oxidation of toluene to amide without oxidation to carboxylic acid. This reaction involves metal-free oxidation, a mild reaction condition and tert-butyl alcohol as the only by-product.

Graphical abstract: Hypervalent iodine-catalyzed oxidative amidation of methylarenes

Supplementary files

Article information

Article type
Communication
Submitted
07 May 2014
Accepted
20 Jun 2014
First published
20 Jun 2014

RSC Adv., 2014,4, 31817-31820

Author version available

Hypervalent iodine-catalyzed oxidative amidation of methylarenes

K. Azizi, M. Karimi and A. Heydari, RSC Adv., 2014, 4, 31817 DOI: 10.1039/C4RA04215H

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