Benzylic C-H arylation with dicyanoarenes convergent paired electrolysis

• Published in: Green chemistry : an international journal and green chemistry resource : GC Vol. 25; no. 14; pp. 5483 - 5488
• Main Authors: Tang, Shanyu, Vincent, Guillaume
• Format: Journal Article
• Published: 17.07.2023
• ISSN: 1463-9262; 1463-9270
• DOI: 10.1039/d3gc00866e

We describe the convergent paired electrolysis of methylarene derivatives and 1,4-dicyanoarenes to perform the arylative functionalization of a benzylic C(sp 3 )-H bond to form 1,1-biarylmethane derivatives that are found in several drugs and biologically active compounds. This electrochemical process proceeds via the coupling of a benzylic radical or a benzylic carbocation with a 1,4-dicyanoarene radical anion to form the desired C-C bond followed by elimination of the cyanide anion which could be trapped as a cyanhydrin by an aldehyde. These reactive species are produced, respectively, by the oxidation of the benzylic substrate at the anode and the reduction of the dicyanoarene at the cathode. One of the key challenges that we have overcome is avoiding the formation of overoxidized coupling products at the bisbenzylic position of the biarylmethane products obtained. We describe the convergent paired electrolysis of methylarene derivatives and 1,4-dicyanoarenes to perform the arylative functionalization of a benzylic C(sp 3 )-H bond to form 1,1-biarylmethane derivatives.