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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788832Generated: October 27, 2026

Allyl Mercaptan → 4-Allylthioazetidin-2-one

https://huagongshe.com/reaction/1788832

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 was added and the mixture stirred under nitrogen for 30 minutes. 138.7 g of 4-acetoxyazetidin-2-one was added to the mixture over 10 minutes under nitrogen and the reaction mixture was stirred overnight in an air atmosphere. The reaction mixture was 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-ethylacetate, 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 numberUS04684640
Source datasetuspto-grants-1987_08
ORD IDord-dad2eed20186402398cc850a972487d1
Source noteuspto-grants-1987_08