Metal-Free Direct Electrochemical Deoxygenation of Benzylic Alcohols

An operationally simple electrochemical deoxygenation of benzylic alcohols is reported. The one-step, one-pot process is metal-free and is conducted at room temperature in an undivided cell, offering a more sustainable and step-economical alternative to conventional derivatization-cleavage deoxygenation sequences. The applicability of the reaction is demonstrated using an electronically and sterically diverse set of primary, secondary, and tertiary benzylic alcohols; excellent functional-group tolerance is exhibited, permitting the presence of esters, amides, and even unactivated alcohols in the substrate scope. Based on preliminary mechanistic investigations using chemical probes, electroanalytical techniques, and computational studies, the reaction is postulated to proceed via the reaction of an alcohol with a phosphine radical cation that is formed in situ.

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Publication Details

Journal
ACS Sustainable Chemistry & Engineering
Published
2025-12-02
DOI
https://doi.org/10.1021/acssuschemeng.5c08410
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
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article

Metal-Free Direct Electrochemical Deoxygenation of Benzylic Alcohols

Darren A. Walsh, James D. Cuthbertson, Kristaps Ermanis, Alex G. Edmonds
ACS Sustainable Chemistry & Engineering
Radical Photochemical Reactions
article

Metal-Free Direct Electrochemical Deoxygenation of Benzylic Alcohols

Darren A. Walsh, James D. Cuthbertson, Kristaps Ermanis, Alex G. Edmonds
article en

Abstract

An operationally simple electrochemical deoxygenation of benzylic alcohols is reported. The one-step, one-pot process is metal-free and is conducted at room temperature in an undivided cell, offering a more sustainable and step-economical alternative to conventional derivatization-cleavage deoxygenation sequences. The applicability of the reaction is demonstrated using an electronically and sterically diverse set of primary, secondary, and tertiary benzylic alcohols; excellent functional-group tolerance is exhibited, permitting the presence of esters, amides, and even unactivated alcohols in the substrate scope. Based on preliminary mechanistic investigations using chemical probes, electroanalytical techniques, and computational studies, the reaction is postulated to proceed via the reaction of an alcohol with a phosphine radical cation that is formed in situ.

ACS Sustainable Chemistry & EngineeringVol. 13(49)
University of Nottingham (GB)
Openalex Percentile: Top 71%
Radical Photochemical Reactions
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