1. Department of Chemistry, School of Science , Alzahra University , Tehran, Iran;2. Department of Chemistry, Faculty of Science , Bu-Ali-Sina University , Hamadan, Iran
Abstract:
The electrooxidation of catechols (1a–d) in the presence of pyrimidine-2-thiol (3) as a nucleophile in aqueous solution is described. The mechanistic investigations using cyclic voltammetry and controlled potential coulometry indicate that the quinone derived from catechols participates in a Michael addition reaction with pyrimidine-2-thiol to form corresponding catechol derivatives of 6a–d (ECEC). The efficient electrosynthesis of 6a–d has been performed at carbon rod electrodes in an undivided cell in good yield and purity.