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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973154Generated: October 26, 2026

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

https://huagongshe.com/reaction/1973154

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 numberUS03996243
Source datasetuspto-grants-1976_12
ORD IDord-0b35371745844249b70a345e40328c89
Source noteuspto-grants-1976_12