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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283368Generated: November 1, 2026

m-Bromobenzenesulphonyl chloride → HCID 57750916, compound

https://huagongshe.com/reaction/2283368

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Bromobenzenesulphonyl chlorideHCID 17943—
ReactantHCID 20152693HCID 20152693—
SolventPyridineHCID 1049—
ProductHCID 57750916HCID 5775091666.3%

Reaction Steps

A mixture of 3-amino-thiophene-2-sulfonic acid amide (100 mg, 0.56 mmol) and 3-bromo-benzenesulfonyl chloride (97 μL, 0.67 mmol) in anhydrous pyridine (3 mL) was stirred at room temperature for 17 hours. The solvent was removed in vacuo and the residue was taken up in dichloromethane (25 mL). The organic phase was washed with 1 M hydrochloric acid, saturated sodium bicarbonate and brine, dried over sodium sulfate and concentrated under reduced pressure. Purification by column chromatography, using 4-6% methanol in dichloromethane as the eluent, gave 147.6 mg (66% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-967d71b8d8ce488b81e36eff54b42605
Source noteuspto-grants-2015_09