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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444357Generated: October 25, 2026

Dimethylformamide → 3-(Benzyloxy)-4-bromophenol

https://huagongshe.com/reaction/444357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
Reactant4-BromoresorcinolHCID 81105—
ReactantPotassium hydrideHCID 82127—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
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 on 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 numberUS04263438
Source datasetuspto-grants-1981_04
ORD IDord-a76c6bd593a2437a8a2dbde7c1f1c631
Source noteuspto-grants-1981_04