Reaktionsgleichung
Cl.[F:2][C:3]([F:14])([F:13])[O:4][C:5]1[CH:10]=[CH:9][C:8]([NH:11][NH2:12])=[CH:7][CH:6]=1.[CH3:15][CH2:16][O:17][C:18]([CH:20]([C:24]([CH3:26])=O)[C:21]([CH3:23])=O)=[O:19]>>[CH2:16]([O:17][C:18]([C:20]1[C:21]([CH3:23])=[N:12][N:11]([C:8]2[CH:7]=[CH:6][C:5]([O:4][C:3]([F:13])([F:14])[F:2])=[CH:10][CH:9]=2)[C:24]=1[CH3:26])=[O:19])[CH3:15]Komponenten
3
Versuchsvorschrift
In analogy to the procedure described in Example 38A], (4-trifluoromethoxy-phenyl)-hydrazine hydrochloride and ethyl diacetoacetate gave, after extraction (3× Et2O), drying (Na2SO4) and evaporation, the title compound in 72% yield as orange oil. MS: 328.9 (MH+).
Aufarbeitung
- customgave
- extractionafter extraction (3× Et2O)
- customdrying
- custom(Na2SO4) and evaporation
Quellen und Nachweise
- ORD-Eintrag
- ord-ba75282944304bf294184a7360c7e186
- Quelldatensatz
- uspto-grants-2011_07
- Patentnummer
- US07977358B2
Verknüpfte Notizen
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