1604841-88-4Relevant articles and documents
A green electrochemical method for the synthesis of 2-(phenylthio)-1h-benzo[d]imidazole derivatives
Joudaki, Mahsa,Nematollahi, Davood
, p. G133 - G138 (2018)
The electrochemical oxidation of 4,4’-biphenol (4BP) was studied by cyclic voltammetry in the absence and presence of 2-mercaptobenzimidazole (2MB) in aqueous/ethanol (50/50 v/v) mixture, to evaluate whether the electrogenerated 4,4’-diphenoquinone (4BPs
Investigation of electrochemically induced Michael addition reactions of Ortho- and Para-banzoquinones with 2-mercaptobenzimidazole: Application to electrosynthesis
Nematollahi, Davood,Davarani, Saied S. H.,Mirahmadpour, Pari,Varmaghani, Fahimeh
, p. 398 - 402 (2014/05/20)
Electrochemical oxidation of hydroquinone and catechol derivatives (1a-1d) has been studied in the presence of 2-mercaptobenzimidazole (3) as a nucleophile in water/acetonitrile (85/15, v/v) solutions using cyclic voltammetry. Our results indicate that electrogenerated benzoquinone participated in a Michael addition reaction with 2-mercaptobenzimidazole (3) and via an EC mechanism were converted to the corresponding thioimidazole compounds. These products were obtained in good yields using a carbon electrode in an undivided cell.