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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 616727Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/616727

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,5-DichlorothiopheneHCID 18501—
EduktChlorosulfonic acidHCID 24638—
EduktAcetone cardiceHCID 18522661—
Produkt2,5-Dichlorothiophene-3-sulfonyl chlorideHCID 2736094—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04075347
Quelldatensatzuspto-grants-1978_02
ORD IDord-202c4b75f6e242a8ae686f3407338284
Quellennotizuspto-grants-1978_02