Electrochemical Synthesis of Benzotriazoles and Benzotriazinones

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Authors: Shu Zhu, Yi-Chao Lin, Guo-Cai Yuan, Hong Yan, Ke-Yin Ye
Cited by: 1
References: 32

Abstract

Benzotriazoles and benzotriazinones are pivotal N -heterocycles in organic synthesis, drug discovery, and materials science. Herein, we present a safe electrochemical strategy that directly transforms 2-nitroanilines and 2-nitrobenzamides into these heterocycles through in situ nitro reduction and diazotization. By precisely tuning the redox potentials and employing suitable electrodes, unstable diazonium intermediates are generated and consumed in a controlled manner, avoiding their over-reduction. This approach offers a scalable synthetic route directly from nitro precursors.

Fields of Study & Subjects

Nanomaterials for catalytic reactions Radical Photochemical Reactions Quinazolinone synthesis and applications

Publication details

Journal / source
Organic Letters
Publisher
American Chemical Society (ACS)
Volume
28
Issue
15
Pages
4767–4771
Publication date
1 April 2026
Language
EN