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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090523Generated: November 2, 2026

Dimethyl Sulfoxide → 1-Allyloxycarbonyl-3-(2-methyl-3-oxo-1-butenyl)azetidine

https://huagongshe.com/reaction/1090523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
Reactant3-(Triphenyl-lambda~5~-phosphanylidene)butan-2-oneHCID 301922—
Reactant1-Allyloxycarbonyl-3-hydroxymethylazetidineHCID 19914892—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product1-Allyloxycarbonyl-3-(2-methyl-3-oxo-1-butenyl)azetidineHCID 5706663389.1%

Reaction Steps

To a solution of oxalyl chloride (6.3 g) in methylene chloride (85 ml) was added dimethyl sulfoxide (3.87 g) at -60° C. and stirred was stirred for 15 minutes. A solution of 1-allyloxycarbonyl-3-hydroxymethylazetidine (6.8 g) in methylene chloride (21 ml) was then added thereto and the mixture was stirred at -60° C. for 30 minutes. Triethylamine (20 g) was dropwise added thereto. To the mixture was added water (50 ml) and organic layer was separated washed with water, dried over magnesium sulfate, evaporated and coevaporated with benzene to give an oily residue. The residue was dissolved in methylene chloride (160 ml) and 3-triphenylphosphoranylidenebutan-2-one (11.8 g) was added thereto and the mixture was stirred overnight at room temperature. The evaporated residue was triturated with ethyl acetate and the insoluble material was filtered. The filtrate was applied on silica gel column using a mixture of n-hexane and ethyl acetate. The main fractions were evaporated to give 1-allyloxycarbonyl-3-(2-methyl-3-oxo-1-butenyl)azetidine (7.06 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081237
Source datasetuspto-grants-1992_01
ORD IDord-b1ebb0e88b0f4f9aad5867563d7a684c
Source noteuspto-grants-1992_01