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Oxidative Coupling of o-Phenylenediamine with Arylmethylamines to Synthesize Aryl-Substituted Benzimidazoles Under Catalyst-Free and Solvent-Free Conditions

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Version 3 2014-07-09, 01:13
Version 2 2014-07-09, 01:13
Version 1 2014-07-09, 01:13
journal contribution
posted on 2014-07-09, 01:13 authored by Jiatao Yu, Ming Lu

Solvent-free oxidative synthesis of benzimidazoles from arylmethylamines and o-phenylenediamine has been achieved under catalyst-free conditions. This reaction can use tert-butyl hydroperoxide (TBHP) as the oxidant, and a wide variety of derivatives were obtained in good yields. The reaction mechanism was proposed and this method provides a direct and practical approach for the preparation of substituted benzimidazoles.

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