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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636443Generated: November 3, 2026

3-(Phenylmethoxy)benzenemethanol → 3-Benzyloxybenzyl bromide

https://huagongshe.com/reaction/1636443

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Phenylmethoxy)benzenemethanolHCID 74341—
ReactantBromotrimethylsilaneHCID 76113—
SolventDichloromethaneHCID 6344—
Product3-Benzyloxybenzyl bromideHCID 1502047—

Reaction Steps

A solution of 3-benzyloxybenzyl alcohol (9.54 g) in methylene chloride (40 ml) with TMSBr (2.5 eq, 13 mL) was heated at reflux for 1 hr. After cooling, the reaction was concentrated and then reconcentrated 2 X with methylene chloride (40 ml). The residue was chromatographed on silica gel eluting first with hexane followed by 10% methylene chloride in hexane to afford 3-benzyloxybenzyl bromide which solidifies on cooling. 5.75 g m.p. 38°-40°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034118
Source datasetuspto-grants-2000_03
ORD IDord-9d012c84c1c1465e9714932820391b13
Source noteuspto-grants-2000_03