Reduction of nitrobenzene to phenylhydroxylamine with anthraquinone-2-sulfonic sodium as an electron mediator

Abstract

Phenylhydroxylamine (PHA) is a key intermediate for the synthesis of drugs and fine chemicals. However, it is challenging to synthesize PHA with a high selectivity because of the highly unstable nature of the PHA. In this study, we used anthraquinone-2-sulfonic sodium as an electron mediator with the “off-field electrocatalysis” strategy for the reduction of nitrobenzene (NB) and achieved a selectivity as high as 97% at a conversion over 99% of NB to phenylhydroxylamine (PHA).

Graphical abstract: Reduction of nitrobenzene to phenylhydroxylamine with anthraquinone-2-sulfonic sodium as an electron mediator

Supplementary files

Article information

Article type
Communication
Submitted
11 Apr 2025
Accepted
19 May 2025
First published
20 May 2025

Chem. Commun., 2025, Advance Article

Reduction of nitrobenzene to phenylhydroxylamine with anthraquinone-2-sulfonic sodium as an electron mediator

S. Chen, B. Chang, C. Cheng, S. Ye, X. Qu, Q. Wang and C. Li, Chem. Commun., 2025, Advance Article , DOI: 10.1039/D5CC02053K

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