Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389979Generated: October 30, 2026

Potassium Hydroxide → 4-(4-Ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzonitrile

https://huagongshe.com/reaction/389979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant3,4-DifluorobenzonitrileHCID 587203—
Reactant4-Ethyl-5-fluoro-2-methoxyphenolHCID 45933640—
SolventAcetonitrileHCID 6342—
Product4-(4-Ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzonitrileHCID 5103474994.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 4-ethyl-5-fluoro-2-methoxyphenol (1 g, 5.87 mmol), 3,4-difluorobenzonitrile (899 mg, 6.46 mmol) and potassium hydroxide (395 mg, 7.04 mmol) in anhydrous acetonitrile (35 mL) under argon was stirred at 80° C. overnight. The reaction mixture was concentrated under vacuum and diluted with ethyl acetate and a saturated aqueous solution of ammonium chloride. The aqueous layer was separated and extracted twice with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtrated and concentrated in vacuo to give a brown oil (1.6 g). The crude product was purified by flash chromatography on silica gel, using cyclohexane/ethyl acetate (9:1) as eluent. The title product was obtained as a colourless oil that crystallized slowly (1.42 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383621B2
Source datasetuspto-grants-2013_02
ORD IDord-c6f60e1e656e4b88b6db5bd14cf6ab3e
Source noteuspto-grants-2013_02