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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410295Generated: November 2, 2026

Allyl bromide → 1-(Allyloxy)-2-bromo-5-chloro-4-(4-ethoxybenzyl)benzene

https://huagongshe.com/reaction/1410295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-chloro-4-(4-ethoxybenzyl)phenolHCID 71117194—
SolventAcetoneHCID 180—
Product1-(Allyloxy)-2-bromo-5-chloro-4-(4-ethoxybenzyl)benzeneHCID 8672858295%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 2-Bromo-5-chloro-4-(4-ethoxybenzyl)phenol (7, 55 mmol) in acetone (180 mL) were added potassium carbonate (15.2 g, 110 mmol) and allyl bromide (7 mL, 83 mmol) and heated at 65° C. for 3 h. The insoluble material was removed by filter and the filtrate was evaporated under reduced pressure. The crude residue was purified on Biotage® purification apparatus (silica gel, 3 to 10% ethyl acetate in hexanes) to yield the title compound (21 g, 52 mmol, 95%) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921412B2
Source datasetuspto-grants-2014_12
ORD IDord-92f298d08a9e4a669cd2a312da931b70
Source noteuspto-grants-2014_12