Reaktion #482800

ord-45ac57ca6cbb4eb1913bf30e3a6ba038

Reaktionsgleichung

Cc1ccccc1OCCCc1oc(Cl)nc1-c1ccc(Cl)cc1
2-chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazole
CCc1ncc[nH]1
2-ethylimidazole
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CN(C)C=O
N,N-dimethylformamide
CCc1nccn1-c1nc(-c2ccc(Cl)cc2)c(CCCOc2ccccc2C)o1
4-(4-chlorophenyl)-2-(2-ethyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole
Ausbeute 38.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
125°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationthe solid precipitate was filtered
  2. 2
    Sonstigeair-dried
  3. 3
    Sonstigerecrystallized from acetone-isopropyl ether

Vorschrift

A mixture of 2-chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazole (1.00 g), 2-ethylimidazole (960 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 the solid precipitate was filtered, air-dried and recrystallized from acetone-isopropyl ether to give 4-(4-chlorophenyl)-2-(2-ethyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole as pale yellow prisms (438 mg, 38%). Melting point 91-92° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06605629B1uspto-grants-2003_08