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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621257Generated: October 27, 2026

Triethylamine → 3-(Methoxy)-4-(benzyloxy)benzyl methanesulfonate

https://huagongshe.com/reaction/1621257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Benzyloxy-3-methoxybenzyl alcoholHCID 98832—
SolventDichloromethaneHCID 6344—
Product3-(Methoxy)-4-(benzyloxy)benzyl methanesulfonateHCID 57594645—

Reaction Steps

A solution of 3-(methoxy)-4-(benzyloxy)benzyl alcohol (0.244 g, 1.00 mmol) in CH2Cl2 (2.0 mL) was treated with methanesulfonylchloride (0.085 mL, 1.10 mmol) and Et3N (0.160 mL, 1.15 mmol). After stirring 1 h at ambient temperature, the reaction mixture was filtered through a short plug of silica gel using CH2Cl2 as the eluant. The solution was concentrated in vacuo and taken on without purification. MS (ES+) m/e 323 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772507B2
Source datasetuspto-grants-2014_07
ORD IDord-d9d9cfa8f29c4b7e9be889d9b8217100
Source noteuspto-grants-2014_07