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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894912Generated: October 25, 2026

Water → 3-(Benzyloxy)-4-bromophenol

https://huagongshe.com/reaction/894912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
Reactant4-BromoresorcinolHCID 81105—
ReactantPotassium hydrideHCID 82127—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product3-(Benzyloxy)-4-bromophenolHCID 15670654—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. slurry of 1.7 g. (42.5 mmoles) of potassium hydride in 35 ml of N,N-dimethylformamide is slowly added a solution of 7.22 g. (38.2 mmoles) of 4-bromoresorcinol. The resultant mixture is stirred for 30 minutes and then 4.54 ml. (38.2 mmoles) of benzyl bromide is slowly added. The reaction mixture is stirred 3 hours longer at 0° C. and then added to 200 ml. of cold water and 200 ml. of ether. The ether extract is washed twice with 200 ml. portions of water, dried over magnesium sulfate and evaporated to an oil. The crude oil is purified via column chromatography an 400 g. of silica gel eluted with 25% ether-pentane to yield (in order of elution) 2.2 g. (16%) of 2,4-dibenzyloxybromobenzene, 0.21 g. (2%) of 5-benzyloxy-2-bromophenol and 3.52 g. (33%) of 3-benzyloxy-4-bromophenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284829
Source datasetuspto-grants-1981_08
ORD IDord-5d869485a50349e9bb706649529f7753
Source noteuspto-grants-1981_08