Issue 14, 2023

Benzylic C–H arylation with dicyanoarenes via convergent paired electrolysis

Abstract

We describe the convergent paired electrolysis of methylarene derivatives and 1,4-dicyanoarenes to perform the arylative functionalization of a benzylic C(sp3)–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.

Graphical abstract: Benzylic C–H arylation with dicyanoarenes via convergent paired electrolysis

Supplementary files

Article information

Article type
Paper
Submitted
14 Marts 2023
Accepted
19 Jūn. 2023
First published
21 Jūn. 2023
This article is Open Access
Creative Commons BY license

Green Chem., 2023,25, 5483-5488

Benzylic C–H arylation with dicyanoarenes via convergent paired electrolysis

S. Tang and G. Vincent, Green Chem., 2023, 25, 5483 DOI: 10.1039/D3GC00866E

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