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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411828Generated: October 25, 2026

Water → 4-(3-Trifluoromethylphenoxy)-2-(4-Trifluoromethylphenyl)-Pyrimidine

https://huagongshe.com/reaction/411828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantPotassium CarbonateHCID 11430—
Reactant3,3-Dichloro-2-propenalHCID 17554—
Reactant1,1,1,3-Tetrachloro-3-ethoxypropaneHCID 12350822—
Reactant4-(Trifluoromethyl)benzamidine HydrochlorideHCID 12535791—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(3-Trifluoromethylphenoxy)-2-(4-Trifluoromethylphenyl)-PyrimidineHCID 992995080%

Reaction Steps

Water (20 mmoles) is added to a solution of 1,1,1,3-tetrachloro-3-ethoxypropane (10 mmoles) in dimethoxyethane (25 ml). The reaction mixture is stirred for 2 h under reflux. The resulting mixture is slowly added to a mixture consisting of a 4-trifluoromethylbenzamidine hydrochloride (10 mmoles), 3-trifluoromethylphenol (11 mmoles), potassium carbonate (60 mmoles) and dimethoxyethane (50 ml), which is stirred under reflux. When the addition of 3,3-dichloroacrolein solution is completed additional 4-trifluoromethylbenzamidine hydrochloride (1 mmoles) is added. The reaction mixture is stirred for 2 hours under reflux and subsequently cooled down to ambient temperature, filtered through silica, and the organic phase is concentrated in vacuo. The residue is purified by chromatography on SiO2 (petrol ethers/diisopropylether: 6/1) to yield 3,07 g (80%) of the product having a melting point of 66-67° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559307B2
Source datasetuspto-grants-2003_05
ORD IDord-c34d230f252a4708b6320892160c65d1
Source noteuspto-grants-2003_05