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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603744Generated: October 31, 2026

2-(Benzyloxy) ethanol → 2-Benzyloxyethyl mesylate

https://huagongshe.com/reaction/1603744

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzyloxy) ethanolHCID 12141—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product2-Benzyloxyethyl mesylateHCID 10857272—

Reaction Steps

To a solution of 2-(benzyloxy)ethanol in 320 ml of dichloromethane, 35 ml of triethylamine and 19.5 ml of methanesulfonyl chloride were added under ice cooling, followed by stirring at room temperature for 2 hours. The reaction mixture was added with ice water and then extracted with dichloromethane. After the extract was washed with a saturated solution of sodium chloride, the extract was dried over magnesium sulfate and then filtered. The filtrate was concentrated under reduced pressure, whereby 49 g of 2-(benzyloxy)ethyl methanesulfonate were obtained (yield: stoichiometric).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990139
Source datasetuspto-grants-1999_11
ORD IDord-26a9a54b5b09499695ec5eb3ca57f1ee
Source noteuspto-grants-1999_11