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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616727Generated: October 26, 2026

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

https://huagongshe.com/reaction/616727

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 numberUS04075347
Source datasetuspto-grants-1978_02
ORD IDord-202c4b75f6e242a8ae686f3407338284
Source noteuspto-grants-1978_02