Oxindole → 3-(3,5-Diisopropyl-4-methoxybenzylidene)-1,3-dihydroindol-2-one
Reaction equation
[CH:1]([C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([CH:14]([CH3:16])[CH3:15])[C:11]=1[O:12][CH3:13])[CH:7]=O)([CH3:3])[CH3:2].[NH:17]1[C:25]2[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH2:19][C:18]1=[O:26]>>[CH:1]([C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([CH:14]([CH3:16])[CH3:15])[C:11]=1[O:12][CH3:13])[CH:7]=[C:19]1[C:20]2[C:25](=[CH:24][CH:23]=[CH:22][CH:21]=2)[NH:17][C:18]1=[O:26])([CH3:3])[CH3:2]Participants
3
Procedure
3,5-Diisopropyl-4-methoxybenzaldehyde was then condensed with 2-oxindole to give 0.25 g of 3-(3,5-Diisopropyl-4-methoxybenzylidene)-1,3-dihydroindol-2-one as a yellow-orange solid.
Sources & evidence
- ORD record
- ord-baac72e6acb944ae8b7d03a7653ebd4a
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06855730B2
Reaction notes
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