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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1730067Erstellt: 26. Oktober 2026

3-Methylthiophene → 3-Methylthiophene-2-sulfonyl chloride

https://huagongshe.com/reaction/1730067

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-MethylthiopheneHCID 12024—
EduktChlorosulfonic acidHCID 24638—
LösungsmittelChloroformHCID 6212—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt3-Methylthiophene-2-sulfonyl chlorideHCID 13425713—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A 49-g (0.5 mol) sample of 3-methylthiophene was added in small portions to a cooled solution (-20° C) of 128 g (1 mol) chlorosulfonic acid in 250 cc chloroform. After the addition was completed, the reaction mixture was allowed to warm to about 25° C and then heated at reflux for 30 minutes. The reaction mixture was then diluted with ice water and neutralized with aqueous sodium bicarbonate solution. The organic layer was separated, dried over magnesium sulfate and evaporated to give 30 g of 3-methyl-2-thienylsulfonyl chloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03991081
Quelldatensatzuspto-grants-1976_11
ORD IDord-daee733669fe41d397471f0f084a84c8
Quellennotizuspto-grants-1976_11