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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980628Generated: October 27, 2026

Allyl Mercaptan → 4-Allylthioazetidin-2-one

https://huagongshe.com/reaction/1980628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl MercaptanHCID 13367—
ReactantSodium HydroxideHCID 14798—
Reactant4-Acetoxy-2-azetidinoneHCID 119981—
SolventWaterHCID 962—
Product4-Allylthioazetidin-2-oneHCID 12849630—

Reaction Steps

A solution of 42.9 g of sodium hydroxide in 500 ml of water was made up under nitrogen and cooled to room temperature, 108 ml of allyl mercaptan were added and the mixture stirred under nitrogen for 30 minutes. 138.7 g of 4-acetoxyazetidin-2-one were added to the mixture over 10 minutes under nitrogen and the reaction mixture was stirred overnight. The reaction was checked for completion by T.L.C. (hexane-ethyl acetate) and extracted into dichloromethane (6×250 ml). The organic layer was washed with water (2×250 ml), dried over magnesium sulphate and evaporated in vacuo to dryness. Purification, over silica gel and elution with hexane-ethyl acetate afforded the above product as a yellow oil. (112.1 g, 73% of the theoretical yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510086
Source datasetuspto-grants-1985_04
ORD IDord-d666fe79e1714a0eb1158ae20093c54f
Source noteuspto-grants-1985_04