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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730202Generated: November 1, 2026

Acetone → 1-Fluoro-4-(prop-2-en-1-yloxy)benzene

https://huagongshe.com/reaction/1730202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantAllyl bromideHCID 7841—
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
Product1-Fluoro-4-(prop-2-en-1-yloxy)benzeneHCID 637342—

Reaction Steps

A mixture of 336.3 parts of 4-fluorophenol, 417.5 parts of allyl bromide, 420 parts of potassium carbonate and 480 parts of acetone is stirred and refluxed for 8 hours. After cooling to room temperature, 2250 parts of water are added. The aqueous layer is separated and extracted twice with ether. The combined extracts are washed successively twice with sodium hydroxide solution 10% and twice with sodium chloride solution, dried over potassium carbonate, filtered and evaporated. The oil residue is distilled in vacuo, yielding 381.8 parts of 4-allyloxy-fluorobenzene; bp. 93° C at 23 mm. pressure; nD20 : 1.4950;d2020 : 1.070.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03991202
Source datasetuspto-grants-1976_11
ORD IDord-32abde345f2d4b4a99ab3343ae102ad0
Source noteuspto-grants-1976_11