Issue 23, 2014

Metal catalyst free one-pot synthesis of 2-arylbenzimidazoles from α-aroylketene dithioacetals

Abstract

An efficient green synthetic approach has been developed towards the synthesis of 2-aryl substituted benzimidazoles from α-aroylketene dithioacetals (AKDTAs) 1 and o-phenylenediamine (OPD) 2. The reaction has been achieved in water with a catalytic amount of acetic acid. 2-Arylbenzimidazoles have been synthesized in remarkable yields under both thermal and microwave conditions. The metal catalyst free condition makes this transformation very green, practical and attractive.

Graphical abstract: Metal catalyst free one-pot synthesis of 2-arylbenzimidazoles from α-aroylketene dithioacetals

Supplementary files

Article information

Article type
Paper
Submitted
18 Dec 2013
Accepted
06 Jan 2014
First published
07 Jan 2014

RSC Adv., 2014,4, 12028-12036

Author version available

Metal catalyst free one-pot synthesis of 2-arylbenzimidazoles from α-aroylketene dithioacetals

P. Dhanalakshmi, S. Thimmarayaperumal and S. Shanmugam, RSC Adv., 2014, 4, 12028 DOI: 10.1039/C3RA47761D

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