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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105276Generated: November 1, 2026

Benzenesulfonyl chloride → methyl 3-[(phenylsulfonyl)amino]thiophene-2-carboxylate

https://huagongshe.com/reaction/2105276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Productmethyl 3-[(phenylsulfonyl)amino]thiophene-2-carboxylateHCID 443039292.4%

Reaction Steps

Methyl 3-aminothiophene-2-carboxylate (3.14 g, 20 mmol) was dissolved in pyridine (10 mL) at room temperature. The flask was sealed with a septum and a nitrogen inlet. The solution was treated slowly with a benzenesulfonyl chloride (2.5 mL, 19.5 mmol). The reaction was followed by thin layer chromatography. The reaction was diluted with ethyl acetate and washing with 2N HCl. The organic layer was washed with saturated, aqueous sodium chloride solution and dried over sodium sulfate. The solution was decanted and evaporated under reduced pressure to give 3-benzenesulfonylaminothiophene-2-carboxylic acid methyl ester (5.36 g, 90%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579340B2
Source datasetuspto-grants-2009_08
ORD IDord-a483d695833f4299ae245d81c15cea62
Source noteuspto-grants-2009_08