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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980958Generated: November 1, 2026

HCID 86741247, compound → HCID 70434617, compound

https://huagongshe.com/reaction/980958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86741247HCID 86741247—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 70434617HCID 70434617—

Reaction Steps

Sulphuryl chloride (59.7 mg, 35.8 μl, 0.442 mmole) was added to a solution of methyl 2-(4-methylthio-2-azetidinon-1-yl)-2-(4-trifluoromethyl-4-hydroxy-1,3-dithiolan-2-ylidene)acetate (166 mg, 0.442 mmole) in methylene chloride (3 ml) at room temperature, with stirring. After this addition, the solution was stirred for 3 minutes and then the solvent was distilled off to give the crude methyl 2-(4-chloro-2-azetidinon-1-yl)-2-(4-trifluoromethyl-4-hydroxy-1,3-dithiolan-2-ylidene)acetate. This 4-chloroazetidinone compound was dissolved in methylene chloride (3 ml) without purification, and triethylamine (185 μl) was added thereto, after which the mixture was stirred at room temperature for 2 hours. The solvent was distilled off from the reaction mixture under reduced pressure. The resulting residue was dissolved in ethyl acetate and washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulphate. The solvent was distilled off under reduced pressure and the residue was purified by preparative thin layer chromatography (eluent: a 3:2 by volume mixture of benzene and ethyl acetate), to give 63 mg of the desired product as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04639441
Source datasetuspto-grants-1987_01
ORD IDord-9f27a9fc2c4b477fbc9ad5a72a176e34
Source noteuspto-grants-1987_01