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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973913Generated: October 29, 2026

2,5-Dichlorothiophene → 2,5-Dichlorothiophene-3-sulfonyl chloride

https://huagongshe.com/reaction/1973913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DichlorothiopheneHCID 18501—
ReactantChlorosulfonic acidHCID 24638—
ReactantAcetone cardiceHCID 18522661—
Product2,5-Dichlorothiophene-3-sulfonyl chlorideHCID 2736094—

Reaction Conditions

Temperature50 °C

Reaction Steps

A 96.8-g (0.632 mol) sample of 2,5-dichlorothiophene was added dropwise to a cooled (dry ice/acetone bath, about -10° to -15° C) and stirred solution of 163 g (1.39 mol) of chlorosulfonic acid. After the addition was completed, the reaction mixture was stirred at 50° C for 2 hours, cooled, and then poured into 200 g of ice. The aqueous reaction mixture was extracted with methylene chloride. The methylene chloride extract was washed with saturated aqueous sodium bicarbonate solution, washed with water, dried over magnesium sulfate, and evaporated to give 87 g of 2,5-dichloro-3-thienylsulfonyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998961
Source datasetuspto-grants-1976_12
ORD IDord-5aa08ce7d34a43beb392a9940c15e853
Source noteuspto-grants-1976_12