Facile access to thioethers using sodium thiosulfate as the sulfur surrogate under base-mediated conditions

Abstract

In this study, we developed an efficient synthetic method for thioether formation from sodium thiosulfate and organic bromides under transition-metal- and oxidant-free conditions. Sodium thiosulfate served as the sulfur source, reacting with an organic bromide to generate a Bunte salt; this salt subsequently reacted with the organic bromide through the in situ generation of a thiolate. The advantages of this method include operational simplicity, the production of structurally diverse compounds with favorable yields, the use of odorless and low-toxicity reagents, and straightforward applicability to large-scale operations.

Graphical abstract: Facile access to thioethers using sodium thiosulfate as the sulfur surrogate under base-mediated conditions

Supplementary files

Article information

Article type
Paper
Submitted
11 May 2026
Accepted
28 May 2026
First published
29 May 2026

Org. Biomol. Chem., 2026, Advance Article

Facile access to thioethers using sodium thiosulfate as the sulfur surrogate under base-mediated conditions

C. Wu, C. Yang, T. Sung, T. Chen, P. Lin and C. Liang, Org. Biomol. Chem., 2026, Advance Article , DOI: 10.1039/D6OB00749J

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