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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566195Generated: November 2, 2026

Allyl bromide → 5-Allyloxy-4-bromo-2-fluoroaniline

https://huagongshe.com/reaction/566195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Amino-2-bromo-4-fluorophenolHCID 10965651—
SolventAcetonitrileHCID 6342—
Product5-Allyloxy-4-bromo-2-fluoroanilineHCID 2126559832.9%

Reaction Steps

5-Amino-2-bromo-4-fluorophenol (30.9 g), allyl bromide (21.8 g) and potassium carbonate (22.77 g) were suspended in acetonitrile (300 ml), and the mixture was stirred at room temperature for 12 hours. After the reaction, the precipitates were filtered, the solvent was distilled off, and this was extracted with ethyl acetate. After washing with water, it was dried over anhydrous magnesium sulfate. Then, ethyl acetate was distilled off and the resulting oily substance was purified by chromatography on silica gel (ethyl acetate:n-hexane=1:3) to obtain the objective 5-allyloxy-4-bromo-2-fluoroaniline (12.14 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174839B1
Source datasetuspto-grants-2001_01
ORD IDord-b3d8c62272b443e0bc028e62b5887f53
Source noteuspto-grants-2001_01