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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395625Erstellt: 24. Oktober 2026

Dimethylformamide → 4-(4-Chlorophenyl)-5-[3-(2-methylphenoxy)propyl]-2-(2-phenyl-1-imidazolyl)oxazole

https://huagongshe.com/de/reaction/395625

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
Edukt2-PhenylimidazoleHCID 69591—
Edukt2-Chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazoleHCID 10882967—
LösungsmittelWaterHCID 962—
Produkt4-(4-Chlorophenyl)-5-[3-(2-methylphenoxy)propyl]-2-(2-phenyl-1-imidazolyl)oxazoleHCID 18174764—

Reaktionsbedingungen

Temperatur125 °C

Reaktionsschritte

A mixture of 2-chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazole (1.00 g), 2-phenylimidazole (432 mg), potassium carbonate (1.38 g) and N,N-dimethylformamide (10 ml) was stirred at 120-130° C. for 1 hour. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate (10 ml×2). The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography, and 4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]-2-(2-phenyl-1-imidazolyl)oxazole was obtained as an oil (512 mg, 39%) from an ethyl acetate-hexane (1:1, v/v)-eluted fraction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605629B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-4da66639a19a4e26abf714bbf6293d9d
Quellennotizuspto-grants-2003_08