Oxidative Functionalization of Amines Using an Electrocatalytic Aminoxyl‐Mediated Reaction: Preparation of <i>N</i> ‐Benzylidenebenzylamines from Benzylamines

A methodology is reported for the preparation of imines from amines by means of an electrocatalytic aminoxyl‐mediated reaction. It is performed using readily available electrodes in a commercially available electrochemistry apparatus and does not require the use of a reference electrode. The methodology proceeds under mild conditions and delivers good to excellent isolated yields across a range of structurally diverse benzyl amines. Selectivity is high, with imines obtained in preference to the more commonly reported nitriles, and the process is readily scalable to the gram level. Operational simplicity and short reaction times make this method a valuable addition to the organic chemist's toolkit.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-10-08
DOI
https://doi.org/10.1002/ejoc.202500720
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Oxidative Functionalization of Amines Using an Electrocatalytic Aminoxyl‐Mediated Reaction: Preparation of N ‐Benzylidenebenzylamines from Benzylamines

Chelsea M. Schroeder, Nicholas E. Leadbeater, Ashly Gasior
European Journal of Organic Chemistry
Radical Photochemical Reactions
article

Oxidative Functionalization of Amines Using an Electrocatalytic Aminoxyl‐Mediated Reaction: Preparation of N ‐Benzylidenebenzylamines from Benzylamines

Chelsea M. Schroeder, Nicholas E. Leadbeater, Ashly Gasior
article en

Abstract

A methodology is reported for the preparation of imines from amines by means of an electrocatalytic aminoxyl‐mediated reaction. It is performed using readily available electrodes in a commercially available electrochemistry apparatus and does not require the use of a reference electrode. The methodology proceeds under mild conditions and delivers good to excellent isolated yields across a range of structurally diverse benzyl amines. Selectivity is high, with imines obtained in preference to the more commonly reported nitriles, and the process is readily scalable to the gram level. Operational simplicity and short reaction times make this method a valuable addition to the organic chemist's toolkit.

European Journal of Organic ChemistryVol. 28(40)
University of Connecticut (US)
Openalex Percentile: Top 78%
Radical Photochemical Reactions
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Oxidative Functionalization of Amines Using an Electrocatalytic Aminoxyl‐Mediated Reaction: Preparation of <i>N</i> ‐Benzylidenebenzylamines from Benzylamines — Chelsea M. Schroeder, Nicholas E. Leadbeater, et al. · European Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS