Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257130Generated: October 25, 2026

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

https://huagongshe.com/reaction/257130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,2,3-Benzothiadiazol-7-ylmethanolHCID 20096433—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product7-Methylsulfonyloxymethylbenzo-1,2,3-thiadiazoleHCID 20096456—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260423
Source datasetuspto-grants-1993_11
ORD IDord-d3bf367c5b404175b43a123d4f5cba0a
Source noteuspto-grants-1993_11