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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081738Generated: October 25, 2026

Phenoxyethanol → 2-Phenoxyethyl methanesulfonate

https://huagongshe.com/reaction/1081738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenoxyethanolHCID 31236—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventDichloromethaneHCID 6344—
Product2-Phenoxyethyl methanesulfonateHCID 226499—

Reaction Steps

To a solution of 2-(phenoxy)ethanol (1.35 g, 9.78 mmoles) and triethytamine (2.04 ml, 14.7 mmoles) in methylene chloride (30 ml) was added methanesulfonyl chloride (0.91 ml, 12 mmoles) with stirring under ice-cooling and the mixture was further stirred under ice-cooling for 10 minutes. The reaction solution was washed with water and the aqueous layer was extracted with methylene chloride (30 ml×3). The methylene chloride layers were combined and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was subjected to column chromatography [eluent:hexane/methyl (1:1)] to obtain crude 1-methanesulfonyloxy-2-(phenoxy)ethane as a pale yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-380e9b64d229418fb0937079369e01fb
Source noteuspto-grants-1996_12