Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414122Generated: October 26, 2026

Water → Benzyl 2-(3-phenoxyacetamido-4-benzenesulfonylthio-2-azetidinone-1-yl)-3-chloromethyl-3-butenate

https://huagongshe.com/reaction/414122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorine monoxideHCID 24646—
ReactantBenzyl 2-(3-phenoxyacetamido-4-benzenesulfonylthio-2-azetidinon-1-yl)-3-methyl-3butenoateHCID 13170072—
SolventCarbon TetrachlorideHCID 5943—
SolventGlycol monoethyl ether acetateHCID 8095—
ProductBenzyl 2-(3-phenoxyacetamido-4-benzenesulfonylthio-2-azetidinone-1-yl)-3-chloromethyl-3-butenateHCID 1317007495%

Reaction Steps

A 200 mg quantity of benzyl 2-(3-phenoxyacetamido-4-benzenesulfonylthio-2-azetidinone-1-yl)-3-methyl-3-butenate was dissolved in 5 ml of ethoxyethyl acetate. The solution was cooled in an ice bath with stirring. Thereto was added dropwise over 10 minutes 1.21 ml of a 0.285M solution of Cl2O in carbon tetrachloride. Water was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate and dried over anhydrous magnesium sulfate. The solvent was distilled off at reduced pressure. The resulting residue was separated and purified by silica gel column chromatography, giving 202 mg of benzyl 2-(3-phenoxyacetamido-4-benzenesulfonylthio-2-azetidinone-1-yl)-3-chloromethyl-3-butenate in 95% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04789740
Source datasetuspto-grants-1988_12
ORD IDord-0fcebac8a6174d4a9b02f6bd61b11380
Source noteuspto-grants-1988_12