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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263830Generated: November 2, 2026

Acetone → 2-(p-Bromophenoxy)ethanol

https://huagongshe.com/reaction/263830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant4-BromophenolHCID 7808—
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
Product2-(p-Bromophenoxy)ethanolHCID 9916844.3%

Reaction Steps

In a reactor, 10.0 g of 4-bromophenol, 7.95 g of ethylene bromohydrin, 16.0 g of K2CO3, and 300 ml of acetone were charged, and stirred and refluxed for 50 hours to give a reaction solution. The reaction solution was poured into water, extracted with toluene, washed with water, and thereafter dried over sodium sulfate anhydride, and the solvent was evaporated and the residue was distilled under reduced pressure in GTO (glass tube oven) to give 5.55 g (Y., 44.3%) of 1-bromo-4-(2-hydroxyethoxy)benzene. GC; 96.8% b.p.; 100° C./0.1 mmHg (which was the prescribed temperature of GTO)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05645760
Source datasetuspto-grants-1997_07
ORD IDord-1dfc2e3ea3d44d62af1b49fe2e86566a
Source noteuspto-grants-1997_07