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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378889Generated: November 1, 2026

4-Bromophenol → 1-bromo-4-(1-ethoxyethoxy)benzene

https://huagongshe.com/reaction/1378889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenolHCID 7808—
ReactantEthyl vinyl etherHCID 8023—
ReactantSodium BicarbonateHCID 516892—
CatalystBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
SolventDichloromethaneHCID 6344—
Product1-bromo-4-(1-ethoxyethoxy)benzeneHCID 2723761100%

Reaction Steps

p-Bromophenol (50 g, 0.29 mole), ethyl vinyl ether (41.7 g, 0.58 mole) and pyridinium p-toluene-sulfonate (1.5 g) were dissolved in methylene chloride (300 ml), followed by reaction with stirring at room temperature for 6 hours. Then 5% aqueous sodium bicarbonate (400 ml) was added to the reaction mixture, and stirred. Then, the organic layer was separated, washed with H2O (300 ml×3), dried over anhydrous MgSO4 and evaporated. The residue (82 g) was distilled under reduced pressure to give 71.1 g of p-bromo-(1-ethoxy-ethoxy)benzene as a pale yellow oil having a boiling point of 112°-114° C./6 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670299
Source datasetuspto-grants-1997_09
ORD IDord-c4a55bdc847848abb0ce74abd2e5db71
Source noteuspto-grants-1997_09