Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257130Erstellt: 24. Oktober 2026

Triethylamine → 7-Methylsulfonyloxymethylbenzo-1,2,3-thiadiazole

https://huagongshe.com/de/reaction/257130

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt1,2,3-Benzothiadiazol-7-ylmethanolHCID 20096433—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt7-Methylsulfonyloxymethylbenzo-1,2,3-thiadiazoleHCID 20096456—

Reaktionsschritte

To a solution of 3.32 g of 7-hydroxymethylbenzo-1,2,3-thiadiazole, 3.1 ml of triethylamine and 0.2 g of 4-dimethylaminopyridine in 50 ml of methylene chloride there is added dropwise with cooling at -5° to 0° C. a solution of 2.23 g of methanesulfonyl chloride in 15 ml of dichloromethane, and the mixture is stirred for 2 hours at room temperature. The reaction mixture is then treated with ice-water and extracted several times using dichloromethane. The combined extracts are washed with water, dried and evaporated. Chromatographic purification on silica gel (CH2Cl2) gives the title compound as a viscous resin.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05260423
Quelldatensatzuspto-grants-1993_11
ORD IDord-d3bf367c5b404175b43a123d4f5cba0a
Quellennotizuspto-grants-1993_11