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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59740Generated: October 30, 2026

Methanesulfonyl chloride → Ethyl 4-(methylsulfonamido)thiophene-2-carboxylate

https://huagongshe.com/reaction/59740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthyl 4-aminothiophene-2-carboxylateHCID 22418292—
SolventPyridineHCID 1049—
ProductEthyl 4-(methylsulfonamido)thiophene-2-carboxylateHCID 86703842—

Reaction Steps

To a solution of ethyl 4-aminothiophene-2-carboxylate (Int. 41) (theoretical 1.785 mmol) in pyridine (20 ml), methanesulfonyl chloride (0.239 ml, 3.07 mmol) was added and the mixture was stirred overnight at RT. The solvent was evaporated and the residue was partitioned between 1N HCl and EtOAc; the aqueous phase was extracted with EtOAc and the combined organic layers were dried over sodium sulfate and evaporated to afford ethyl 4-(methylsulfonamido)thiophene-2-carboxylate (Int. 42) which was used without any additional purification (370 mg, 1.484 mmol, MS/ESI+249.8 [MH]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440954B2
Source datasetuspto-grants-2016_09
ORD IDord-17b71bdba61442fb8c25b3ca0c7c4eaa
Source noteuspto-grants-2016_09