4.3 Article

OXIDATIVE COUPLING OF O-PHENYLENEDIAMINE WITH ARYLMETHYLAMINES TO SYNTHESIZE ARYL-SUBSTITUTED BENZIMIDAZOLES UNDER CATALYST-FREE AND SOLVENT-FREE CONDITIONS

Journal

SYNTHETIC COMMUNICATIONS
Volume 44, Issue 17, Pages 2520-2528

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/00397911.2014.908310

Keywords

Benzimidazoles; catalyst-free; oxidation; solvent-free; TBHP

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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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