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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899724Generated: November 1, 2026

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

https://huagongshe.com/reaction/1899724

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 layer 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 numberUS05571821
Source datasetuspto-grants-1996_11
ORD IDord-95dc2fe49da741ab8b144f4e26acf500
Source noteuspto-grants-1996_11