Reaktionsgleichung
[CH:1]([C:4]1[C:5]([O:13][CH3:14])=[CH:6][C:7]([CH3:12])=[C:8]([CH:11]=1)[CH:9]=O)([CH3:3])[CH3:2].[CH3:15][C:16]1[CH:24]=[CH:23][CH:22]=[C:21]2[C:17]=1[CH2:18][C:19](=[O:25])[NH:20]2>>[CH:1]([C:4]1[C:5]([O:13][CH3:14])=[CH:6][C:7]([CH3:12])=[C:8]([CH:11]=1)[CH:9]=[C:18]1[C:17]2[C:21](=[CH:22][CH:23]=[CH:24][C:16]=2[CH3:15])[NH:20][C:19]1=[O:25])([CH3:3])[CH3:2]Komponenten
3
Versuchsvorschrift
5-Isopropyl-4-methoxy-2-methylbenzaldehyde was condensed with 4-methyl-2-oxindole to give 0.3 g of 3-(5-isopropyl-4-methoxy-2-methylbenzylidene)-4-methyl-1,3-dihydroindol-2-one as a yellow-orange solid.
Quellen und Nachweise
- ORD-Eintrag
- ord-b2409834628a4ba299ff218a94cce174
- Quelldatensatz
- uspto-grants-2005_02
- Patentnummer
- US06855730B2
Verknüpfte Notizen
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