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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569668Generated: October 26, 2026

Triethylamine → 1,2,3-Thiadiazol-4-ylmethanol methanesulfonate

https://huagongshe.com/reaction/569668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,2,3-Thiadiazol-4-ylmethanolHCID 14727409—
SolventDichloromethaneHCID 6344—
Product1,2,3-Thiadiazol-4-ylmethanol methanesulfonateHCID 5378994571.3%

Reaction Steps

A solution of 1,2,3-thiadiazol-4-ylmethanol (0.75 g, 6.5 mmol) in dichloromethane (20 mL) was cooled to 5° C. under a nitrogen atmosphere and treated with triethylamine (1.018 mL, 7.3 mmol) and methanesulfonyl chloride (0.565 mL, 7.3 mmol). After 15 min, the ice-bath was removed and the reaction mixture was stirred for 2 h. The solution was washed with 1N hydrochloric acid solution (2×2 mL) and water, dried (MgSO4 +MgO) and concentrated. The residue was purified by chromatography (silica gel column 1.5×21 cm) with ether as eluting solvent to give 0.90 g (71%) of 1,2,3-thiadiazol-4-ylmethanol methanesulfonate;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04732977
Source datasetuspto-grants-1988_03
ORD IDord-8499bae8663146e9bbdf2abc9c1fe95f
Source noteuspto-grants-1988_03