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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466534Generated: October 26, 2026

Triethylamine → 2-Phenoxyethyl methanesulfonate

https://huagongshe.com/reaction/1466534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenoxyethanolHCID 31236—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Phenoxyethyl methanesulfonateHCID 22649999%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-phenoxyethanol (10.0 mL, 80.0 mmol) and triethylamine (13.5 mL, 96.9 mmol) in anhydrous CH2Cl2 (250 mL) at 0° C. is added methanesulfonyl chloride (6.80 mL, 87.9 mmol). The resulting cloudy mixture is stirred at 0° C. for 2 h. The mixture is diluted with water (75 mL) and extracted. The organic layer is washed with 1N HCl (75 mL) then saturated NaHCO3/brine (1:1; 75 mL) dried (Na2SO4), filtered, and concentrated. The residue is dried to constant weight under reduced pressure to provide the title compound as a pale yellow oil (17.1 g, 99%). This material is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000043B2
Source datasetuspto-grants-2015_04
ORD IDord-cffced9ee9e14d54820506abb6707b2f
Source noteuspto-grants-2015_04