Reaction equation
[C:1]([C:5]1[CH:6]=[C:7]2[C:12](=[O:13])[O:11][C:9](=O)[C:8]2=[CH:14][CH:15]=1)([CH3:4])([CH3:3])[CH3:2].[CH:16]([C:19]1[CH:25]=[CH:24][CH:23]=[C:22]([CH:26]([CH3:28])[CH3:27])[C:20]=1[NH2:21])([CH3:18])[CH3:17]>>[CH:26]([C:22]1[CH:23]=[CH:24][CH:25]=[C:19]([CH:16]([CH3:18])[CH3:17])[C:20]=1[N:21]1[C:9](=[O:11])[C:8]2=[CH:14][CH:15]=[C:5]([C:1]([CH3:2])([CH3:3])[CH3:4])[CH:6]=[C:7]2[C:12]1=[O:13])([CH3:28])[CH3:27]Participants
3
Procedure
0.605 g of 4-tert-butylphthalic anhydride and 0.630 g of 2,6-diisopropylaniline were mixed, and the mixture was reacted at a temperature of 200° C. for 1 hour.
Workup
- customthe mixture was reacted at a temperature of 200° C. for 1 hour
Sources & evidence
- ORD record
- ord-6ede1dcd7deb4d9ea738934f4e41662a
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06515129B1
Linked notes
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