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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732783Generated: October 31, 2026

Allyl bromide → 3-[4-(4-Chlorophenoxy)phenoxy]-1-propene

https://huagongshe.com/reaction/1732783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Chlorophenoxy)phenolHCID 12346120—
Solvent1-ButanolHCID 263—
Product3-[4-(4-Chlorophenoxy)phenoxy]-1-propeneHCID 10491620100.8%

Reaction Steps

42 g of 4(4-chlorophenoxy)-phenol and 48 g of allyl bromide were heated at the boil at a reflux condenser, while stirring and adding 50 g of potassium carbonate, in 500 ml of butanol for 4 hours. Inorganic salts were then separated from the reaction solution by suction-filtration, the solvent was vaporized and the residue was distilled under greatly reduced pressure. 50 g of 4(4-chlorophenoxy)-phenyl allyl ether were obtained, boiling point: 173°-175° C. under a pressure of 2-3 mm mercury.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04238626
Source datasetuspto-grants-1980_12
ORD IDord-492e3b92ee524260991e03003f06aef7
Source noteuspto-grants-1980_12