5-acetyl-2,3-dihydro-1H-indol-2-one → 5-Acetyl-3-(3,5-diisopropyl-4-methoxybenzylidene)-1,3-dihydroindol-2-one

HRID 24350Notes

Reaction equation

HRID 24350 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].[C:17]([C:20]1[CH:21]=[C:22]2[C:26](=[CH:27][CH:28]=1)[NH:25][C:24](=[O:29])[CH2:23]2)(=[O:19])[CH3:18]>>[C:17]([C:20]1[CH:21]=[C:22]2[C:26](=[CH:27][CH:28]=1)[NH:25][C:24](=[O:29])[C:23]2=[CH:7][C:6]1[CH:5]=[C:4]([CH:1]([CH3:3])[CH3:2])[C:11]([O:12][CH3:13])=[C:10]([CH:14]([CH3:16])[CH3:15])[CH:9]=1)(=[O:19])[CH3:18]

Participants

3

Procedure

3,5-Diisopropyl-4-methoxybenzaldehyde was condensed with 5-acetyl-2-oxindole to give 0.3 g of 5-Acetyl-3-(3,5-diisopropyl-4-methoxybenzylidene)-1,3-dihydroindol-2-one as a yellow-orange solid.

Sources & evidence

ORD record
ord-57356a8340114da2886d20252390e8a0
Source dataset
uspto-grants-2005_02
Patent number
US06855730B2

Reaction notes

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