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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595543Generated: October 31, 2026

Triethylamine → HCID 21704987, compound

https://huagongshe.com/reaction/1595543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-Hydroxyphenethyl alcoholHCID 83404—
SolventDichloromethaneHCID 6344—
ProductHCID 21704987HCID 2170498787.3%

Reaction Steps

9.09 g (79.6 mmole) methanesulfonyl chloride was slowly added to a solution of 5 g (36.2 mmole) 3-hydroxyphenethyl alcohol and 9.14 g (90.5 mmole) triethylamine in 150 ml dichloromethane at 0° C. After stirring at room temperature over night the salts were filtered off, the organic phase was washed with sodium bicarbonate and brine, dried (magnesium sulfate) and evaporated in vacuo to give 9.3 g (yield 87%) of 3-(methylsulfonyloxy)phenethyl methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288096B1
Source datasetuspto-grants-2001_09
ORD IDord-03b3315ceb9149d6bc38ba085dfa21fb
Source noteuspto-grants-2001_09