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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732338Generated: November 1, 2026

Methanesulfonyl chloride → HCID 20306015, compound

https://huagongshe.com/reaction/1732338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(2,6-Dimethoxyphenoxy)ethan-1-olHCID 14257601—
SolventPyridineHCID 1049—
ProductHCID 20306015HCID 2030601540.5%

Reaction Steps

Methanesulphonyl chloride (23 g.) was added dropwise to a stirred solution of 2-[2,6-dimethoxyphenoxy]ethanol (20 g.) (J. Med. Chem. 1969, 12, 326) in pyridine (50 ml.). The solution was left at room temperature for 60 hours, then the solvent evaporated under reduced pressure. The residue was taken up in chloroform, washed with water (3×100 ml.) and sodium bicarbonate solution (5%, 3×100 ml.), dried and the solvent evaporated. The residue was triturated with n-hexane and the solid collected to give 2-[2,6-dimethoxyphenoxy]-ethyl mesylate (11.3 g.) characterized spectroscopically.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237138
Source datasetuspto-grants-1980_12
ORD IDord-0376ac52247c46a4a070b6e6b4f1e4ab
Source noteuspto-grants-1980_12