1-(p-N-tert-butylaminocarbonylphenyl)-4-(1-trityl-4-imidazolyl)-1-butanone → HCID 178509866, Verbindung
Reaktionsgleichung
C([NH:5][C:6]([C:8]1[CH:13]=[CH:12][C:11]([C:14](=[O:42])[CH2:15][CH2:16][CH2:17][C:18]2[N:19]=[CH:20][N:21](C(C3C=CC=CC=3)(C3C=CC=CC=3)C3C=CC=CC=3)[CH:22]=2)=[CH:10][CH:9]=1)=O)(C)(C)C>S(Cl)(Cl)=O>[C:6]([C:8]1[CH:9]=[CH:10][C:11]([C:14](=[O:42])[CH2:15][CH2:16][CH2:17][C:18]2[N:19]=[CH:20][NH:21][CH:22]=2)=[CH:12][CH:13]=1)#[N:5]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 0.5 g of 1-(p-N-tert-butylaminocarbonylphenyl)-4-(1-trityl-4-imidazolyl)-1-butanone in 20 ml of thionyl chloride is refluxed for 3 h and poured into 100 ml of ice-water. The aqueous phase is extracted with ether (3×20 ml), adjusted to pH=10 and reextracted with methylene chloride. The organic phase is dried and evaporated to yield 1-(p-cyanophenyl)-4-(4-imidazolyl)-1-butanone.
Aufarbeitung
- extraction