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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595512Generated: October 25, 2026

Triethylamine → 4-(Methylcarbonyloxy)phenethyl methanesulfonate

https://huagongshe.com/reaction/1595512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzeneethanol, 4-(acetyloxy)-HCID 586676—
SolventDichloromethaneHCID 6344—
Product4-(Methylcarbonyloxy)phenethyl methanesulfonateHCID 2170498997.2%

Reaction Steps

55 g (0.305 mole) 2-(4-methylcarbonyloxyphenyl)-1-ethanol and 34.4 g (0.341 mole) triethylamine in 300 ml dichloromethane were cooled on an ice bath. 38.5 g (0.336 mole) methanesulfonyl chloride was slowly added. The ice bath was removed and the mixture was stirred for 3 hours at room temperature. Water was added and the phases were separated. The organic phase was washed with saturated sodium hydrogen bicarbonate and brine, dried (magnesium sulfate), filtered and evaporated in vacuo to give 76.6 g (yield 97%) of 4-(methylcarbonyloxy)phenethyl methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288096B1
Source datasetuspto-grants-2001_09
ORD IDord-ebd58084eae847f7b137bb1746131eae
Source noteuspto-grants-2001_09