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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420542Generated: November 3, 2026

Allyl Alcohol → HCID 18781991, compound

https://huagongshe.com/reaction/1420542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
Reactant4-Acetoxy-2-azetidinoneHCID 119981—
ReactantSodiumHCID 5360545—
ReactantHCID 18781954HCID 18781954—
SolventEthyl AcetateHCID 8857—
ProductHCID 18781991HCID 1878199148%

Reaction Steps

Sodium (1.15 g) was added to allyl alcohol (50 ml) and this solution treated with allyl 4-(acetylthio)butanoate (10.Og) at room temperature for 20 mins. 4-Acetoxyazetidinone (6.5 g) was added and stirring continued at 20° C. for 1 h The resulting mixture was poured into excess ethyl acetate and the layers separated. The organic layer was washed with water, brine, dried (MgSO4), filtered and evaporated. The residue was chromatographed on silica gel (diethyl ether) to give the title compound as a yellow oil, 5.5 g. 48% yield

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071899
Source datasetuspto-grants-2000_06
ORD IDord-92e768b62bcd474d93a2b9fc36d38b37
Source noteuspto-grants-2000_06