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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270642Generated: November 2, 2026

2-Bromothiophene → 5-Bromothiophene-2-sulfonyl chloride

https://huagongshe.com/reaction/2270642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromothiopheneHCID 13851—
ReactantChlorosulfonic acidHCID 24638—
SolventDichloromethaneHCID 6344—
Product5-Bromothiophene-2-sulfonyl chlorideHCID 273392475%

Reaction Steps

Chlorosulfonic acid was added dropwise over 20 min. to a cold solution (−78° C.) of 2-bromothiophene (16.3 g, 100 mmol) in methylene chloride (50 ml) was added. After addition of chlorosulfonic acid was complete, the cold bath was removed. The reaction mixture was allowed to attain room temperature slowly (2 h), was added dropwise onto the crushed ice (1000 g) and was extracted with methylene chloride (4×100 ml). The combined organic layers was dried over MgSO4, filtered and the solvent was removed under reduced pressure to give a crude product. This was purified by column chromatography using hexane as eluent to give 5-bromothiophene-2-sulfonyl chloride (22 g, 75% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331637B1
Source datasetuspto-grants-2001_12
ORD IDord-0e7e054604da4044a7026e66c85c2787
Source noteuspto-grants-2001_12