Structural effects of the carboxylate anion on Ru-catalyzed C—H arylation of (hetero)aromatic substrates containing N-donor directing group

Anions of carboxylic acids are widely used as the promoters of ruthenium-catalyzed reactions of C—H activation of substrates containing an N-donar directing group. The promoting effect of structure of anions of aliphatic and (hetero)aromatic carboxylic acids on the C—H arylation of benzene, furan, and thiophene rings in benzo[d]imidazol-2-yl-(hetero)arenes, wherein the benzimidazole moiety played the role of N-donor directing group, was evaluated. It was found that the structural effect of carboxylate anion on the efficiency of promotion of the catalytic system can significantly vary upon the arylation of different substrates. Adamantane-1-carboxylic acid was proposed as the most effective and universal promoter, based on which a new efficient catalytic system was developed for the selective arylation of benzo[d]imidazol-2-yl-(hetero)arenes.