Chemoselective, Scalable Nickel-Electrocatalytic O-Arylation of Alcohols

08 July 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.


The formation of aryl-alkyl ether bonds through cross coupling of alcohols with aryl halides represents a useful strategic departure from classical SN2 methods. Numerous tactics relying on Pd-, Cu-, and Ni-based catalytic systems have emerged over the past several years. Herein we disclose a Ni-catalyzed electrochemically driven protocol to achieve this useful transformation with a broad substrate scope in an operationally simple way. This electrochemical method does not require strong base, exogenous expensive transition metal catalysts (e.g. Ir, Ru), and can easily be scaled up in either a batch or flow setting. Interestingly, e-etherification exhibits an enhanced substrate scope over the mechanistically related photochemical variant as it tolerates tertiary amine functional groups in the alcohol nucleophile.


synthetic methodology
aryl etherification

Supplementary materials

Supporting information
Supporting Information containing experimental procedures and characterizations


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