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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 411830Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/411830

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Trifluoromethyl)phenolHCID 7376—
EduktPotassium CarbonateHCID 11430—
Edukt3,3-Dichloro-2-propenalHCID 17554—
Edukt4-Fluorobenzamidine acetateHCID 44784991—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt4-(3-Trifluoromethylphenoxy)-2-(4-fluorophenyl)pyrimidineHCID 986249775,4%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06559307B2
Quelldatensatzuspto-grants-2003_05
ORD IDord-e7c4df2732b2437d9a887a4aae508376
Quellennotizuspto-grants-2003_05