Dodecylsuccinic anhydride → N-(1-heptyloxy-2,2,6,6-tetramethylpiperidin-4-yl)-n-dodecyl succinimide
Reaction equation
[CH2:1]([O:8][N:9]1[C:14]([CH3:16])([CH3:15])[CH2:13][CH:12]([NH2:17])[CH2:11][C:10]1([CH3:19])[CH3:18])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[CH2:20]([CH:32]1[CH2:37][C:36](=O)[O:35][C:33]1=[O:34])[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31]>>[CH2:1]([O:8][N:9]1[C:14]([CH3:16])([CH3:15])[CH2:13][CH:12]([N:17]2[C:36](=[O:35])[CH2:37][CH:32]([CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[C:33]2=[O:34])[CH2:11][C:10]1([CH3:18])[CH3:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7]Participants
3
Procedure
The procedure of Example 75 is repeated using 1-heptyloxy-4-amino-2,2,6,6-tetramethylpiperidine and n-dodecyl succinic anhydride to afford the title compound.
Sources & evidence
- ORD record
- ord-e5032a6f925247fa8a4b622b45ddb378
- Source dataset
- uspto-grants-1993_04
- Patent number
- US05204473
Reaction notes
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