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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351290Generated: November 3, 2026

5-Bromothiophene-2-sulfonyl chloride → 5-BroMo-thiophene-2-sulfonic acid M ethylaMide

https://huagongshe.com/reaction/1351290

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
ReactantMethylamine tetrahydrofuranHCID 66615946—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-BroMo-thiophene-2-sulfonic acid M ethylaMideHCID 1520364—

Reaction Steps

To a solution of 5-bromothiophene-2-sulfonyl chloride (602 mg) in tetrahydrofuran (5 mL) was added dropwise a solution of 2.0M methylamine-tetrahydrofuran (3.5 mL) on an ice bath. After stirring for 15 minutes on an ice bath, the solution was diluted with water and extracted with ethyl acetate. After washing with an aqueous solution of saturated sodium bicarbonate and saturated sodium chloride water, the solution was dried with anhydrous sodium sulfate. After filtration through silica gel, the solvent was removed by evaporation to provide the title compound (608 mg) as a colorless oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217723B2
Source datasetuspto-grants-2007_05
ORD IDord-4099beedcf60446f997ddb36507e5321
Source noteuspto-grants-2007_05