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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156644Generated: November 1, 2026

Water → 1-(2-Bromoethoxy)-4-(2-propenyloxy)benzene

https://huagongshe.com/reaction/1156644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Bromoethoxy)phenolHCID 12833932—
SolventAcetoneHCID 180—
SolventHexaneHCID 8058—
Product1-(2-Bromoethoxy)-4-(2-propenyloxy)benzeneHCID 12941117—

Reaction Steps

To a solution of 45.0 g of 4-(2-bromoethoxy)-phenol (0.207 mol) in 310 ml of acetone was added 54 ml of allyl bromide (0.619 mol) and 45.0 g of anhydrous potassium carbonate (0.326 mol). The reaction mixture was stirred under reflux for eleven hours and was cooled and poured into 2500 ml of water. The mixture was extracted twice with 3:1 ether:methylene-chloride, and the organic layers were washed twice with 1 N NaOH, once with H2O, dried (Na2SO4) and concentrated to dryness under reduced pressure to yield a colorless oil. The analytical sample was prepared by crystallization from hexane to give colorless crystals, mp 27°-28°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04336382
Source datasetuspto-grants-1982_06
ORD IDord-f6c7a7ee5838400a887a6f6e45c899b4
Source noteuspto-grants-1982_06