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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595539Generated: October 29, 2026

Triethylamine → HCID 21704982, compound

https://huagongshe.com/reaction/1595539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHomovanillyl alcoholHCID 16928—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventDichloromethaneHCID 6344—
ProductHCID 21704982HCID 2170498286.6%

Reaction Steps

44 g (0.39 mole) methanesulfonyl chloride was slowly added to a solution of 30 g (0.178 mole) homovanillyl alcohol and 45.3 g (0.45 mmole) triethylamine in 500 ml dichloromethane at −10° 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 50 g (yield 86%) of 3-methoxy-4-(methylsulfonyloxy)phenethyl methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288096B1
Source datasetuspto-grants-2001_09
ORD IDord-af6a52593a144d86b67a51def093643b
Source noteuspto-grants-2001_09