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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411830Generated: October 25, 2026

3-(Trifluoromethyl)phenol → 4-(3-Trifluoromethylphenoxy)-2-(4-fluorophenyl)pyrimidine

https://huagongshe.com/reaction/411830

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantPotassium CarbonateHCID 11430—
Reactant3,3-Dichloro-2-propenalHCID 17554—
Reactant4-Fluorobenzamidine acetateHCID 44784991—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(3-Trifluoromethylphenoxy)-2-(4-fluorophenyl)pyrimidineHCID 986249775.4%

Reaction Steps

3,3-Dichloroacrolein (10 mmoles) diluted with dimethoxyethane (35 ml), is slowly added to a mixture consisting of a 4-fluorobenzamidine acetate (10 mmoles), 3-trifluoromethylphenol (11 mmoles), potassium carbonate (40 mmoles) nd dimethoxyethane (40 ml), which is stirred under reflux. When the addition of 3,3-dichloroacrolein is completed additional 4-fluorobenzamidine acetate (1 mmoles) is added. The reaction mixture is stirred for 3 hours under reflux and subsequently cooled down to ambient temperature over night and filtered through silica. The organic phase is concentrated in vacuo. The residue was purified by chromatography on Al2O3 (petrol ethers/ethyl acetate: 20/1) to yield 2.52 g (75%) of the pure product having a melting point of 52° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559307B2
Source datasetuspto-grants-2003_05
ORD IDord-e7c4df2732b2437d9a887a4aae508376
Source noteuspto-grants-2003_05