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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069689Generated: October 31, 2026

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

https://huagongshe.com/reaction/2069689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant4-FluorophenolHCID 9732—
ReactantSodium HydroxideHCID 14798—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
Product1-Fluoro-4-(prop-2-en-1-yloxy)benzeneHCID 63734297.8%

Reaction Steps

To a solution of 4-fluorophenol (22.4 g, 200 mmol) in DCM (200 mL) was added 50% NaOH (aq) (100 mL), 3-bromoprop-1-ene (26.0 mL, 300.0 mmol) and tetra-n-butylammonium bromide (1.90 g, 6.0 mmol). The suspension was stirred at room temperature for 24 h. The layers were separated and washed with water (2×100 mL), brine (100 mL) and dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography (0-20% EtOAc in hexanes) to provide the desired 1-(allyloxy)-4-fluorobenzene (852) (29.7 g, 97.8%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299117B2
Source datasetuspto-grants-2012_10
ORD IDord-e79c596f88aa4988966e37c036736688
Source noteuspto-grants-2012_10