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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080035Generated: November 1, 2026

Triethylamine → 3-(Benzyloxy)benzyl chloride

https://huagongshe.com/reaction/2080035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-(Phenylmethoxy)benzenemethanolHCID 74341—
SolventDichloromethaneHCID 6344—
Product3-(Benzyloxy)benzyl chlorideHCID 1317349067.5%

Reaction Steps

To a solution of 3-benzyloxybenzyl alcohol (3.0 g, 14.0 mmol) in dichloromethane (30 mL) was added methanesulfonyl chloride (1.39 mL, 16.8 mmol) and triethylamine (2.34 mL, 16.8 mmol) on an ice bath, and the solution was stirred overnight. The reaction solution was diluted with dichloromethane, washed with aqueous solution of 5% sodium bicarbonate, and then, dried over anhydrous magnesium sulfate. The solvent was evaporated, then, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1), and 1-benzyloxy-3-chloromethyl-benzene (2.2 g, 67%) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-ce6f3c562a5d4e2ebe405052503c0bbf
Source noteuspto-grants-2011_04