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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2026 Volume 36, Issue 3, Pages 345–346 (Mi mendc7431)

Communications

Synthesis of secondary thiols from terminal alkenes and P2S5

P. V. Kovyazin, E. R. Palatov, L. V. Parfenova

Institute of Petrochemistry and Catalysis, Ufa Federal Research Centre of the Russian Academy of Sciences, 450075 Ufa, Russian Federation

Abstract: Secondary alkane-2-thiols were obtained through the reaction of terminal alkenes with P2S5 promoted by radical initiators, e.g. TEMPO, AIBN, H2O2 or ButOOH. The yields of 75–86% were achieved by the use of TEMPO in toluene at 80–100 °C or ButOOH in CH2Cl2 at 40 °C.

Keywords: alkane-2-thiols, terminal alkenes, phosphorus pentasulfide, (2,2,6,6-tetramethylpiperidin-1-yl)oxyl, tert-butyl hydroperoxide, free radical reactions, Markovnikov products.

Received: 13.10.2025
Accepted: 18.11.2025

Language: English

DOI: 10.71267/mencom.7936



© Steklov Math. Inst. of RAS, 2026