KBr-Enabled electrochemical transformation of alkynes into α-bromoketones/1,2-diketones

Abstract

In recognition of the crucial role of ketone motifs in significant organic transformations and the synthesis of valuable molecules (e.g., pharmaceuticals, pesticides, and fine chemicals), we herein report an electrochemical protocol for the synthesis of α-bromoketones and 1,2-diketones from alkynes. This method employs safe and cost-effective KBr as both the bromine source and supporting electrolyte, while NFSI acts as an electron acceptor and MeOH serves as the solvent. The transformation proceeds smoothly, delivering the desired products in good yields.

Supplementary files

Article information

Article type
Communication
Submitted
26 Feb 2026
Accepted
31 Mar 2026
First published
01 Apr 2026

Org. Biomol. Chem., 2025, Accepted Manuscript

KBr-Enabled electrochemical transformation of alkynes into α-bromoketones/1,2-diketones

Y. Li, S. Lei and Y. Zhang, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D6OB00329J

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