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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973414Generated: November 2, 2026

Sulfuryl chloride → methyl 2-(acetylamino)-5-chloro-3-thiophenecarboxylate

https://huagongshe.com/reaction/1973414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 2-acetamidothiophene-3-carboxylateHCID 2808565—
SolventChloroformHCID 6212—
Productmethyl 2-(acetylamino)-5-chloro-3-thiophenecarboxylateHCID 818981—

Reaction Steps

To a stirred solution of 19.9 parts of methyl 2-acetamidothiophene-3-carboxylate in 200 parts by volume of chloroform, 8.2 parts by volume of sulfuryl chloride is added dropwise at below 30° C. The mixture is stirred at room temperature for 30 minutes and then cooled with ice. To the mixture, about 300 parts by volume of saturated aqueous sodium bicarbonate solution is cautiously added with stirring. The chloroform layer is separated, washed with water and dried over sodium sulfate. Evaporation of the solvent gives methyl 2-acetamido-5-chlorothiophene-3-carboxylate as crystals. Recrystallization from methanol gives needles melting at 110°-110.5° C. This compound is identical with that obtained in Reference Example 17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03997545
Source datasetuspto-grants-1976_12
ORD IDord-df3983827b9840ff936257e6925977ae
Source noteuspto-grants-1976_12