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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327359Generated: October 29, 2026

4-Bromophenol → Benzene, 1-bromo-4-(hexyloxy)-

https://huagongshe.com/reaction/327359

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenolHCID 7808—
Reactant1-BromohexaneHCID 8101—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
ProductBenzene, 1-bromo-4-(hexyloxy)-HCID 520492—

Reaction Steps

A solution of 1-bromohexane (60 g) in acetone (150 ml) is added dropwise to a stirred mixture of 4-bromphenol (71 g) and K2CO3 (120 g) in acetone 600 ml) at room temperature. The stirred mixture is heated under reflux for 43 hrs (i.e. until glc revealed complete reaction). The product is extracted into ether twice, and the combined ethereal extracts are washed with water, 5% NaOH water and dried (MgSO4). The solvent is removed in vacuo and the residue was distilled (bp=100°-110° C. at 0.1 mm Hg) to yield a colourless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273680
Source datasetuspto-grants-1993_12
ORD IDord-98b4d89affbc4552a6f68b6a40eecafe
Source noteuspto-grants-1993_12