Bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidinyl)decandioate → HCID 53798436, compound
Reaction equation
[C:1]([O:5][CH:6]1[CH2:11][C:10]([CH3:13])([CH3:12])[N:9]([O:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[C:8]([CH3:34])([CH3:33])[CH2:7]1)(=[O:4])[CH:2]=[CH2:3].[C:35]([O:59][CH:60]1[CH2:65][C:64]([CH3:67])([CH3:66])[N:63]([OH:68])[C:62]([CH3:70])([CH3:69])[CH2:61]1)(=[O:58])[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][C:44]([O:46][CH:47]1[CH2:52][C:51]([CH3:54])([CH3:53])[N:50]([OH:55])[C:49]([CH3:57])([CH3:56])[CH2:48]1)=[O:45]>>[C:35]([O:59][CH:60]1[CH2:61][C:62]([CH3:70])([CH3:69])[N:63]([O:68][CH2:3][CH2:2][C:1]([O:5][CH:6]2[CH2:7][C:8]([CH3:33])([CH3:34])[N:9]([O:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[C:10]([CH3:12])([CH3:13])[CH2:11]2)=[O:4])[C:64]([CH3:67])([CH3:66])[CH2:65]1)(=[O:58])[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][C:44]([O:46][CH:47]1[CH2:48][C:49]([CH3:56])([CH3:57])[N:50]([O:55][CH2:3][CH2:2][C:1]([O:5][CH:6]2[CH2:7][C:8]([CH3:33])([CH3:34])[N:9]([O:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[C:10]([CH3:12])([CH3:13])[CH2:11]2)=[O:4])[C:51]([CH3:53])([CH3:54])[CH2:52]1)=[O:45]Participants
3
Procedure
The title compound is prepared from 1-octadecyloxy-2,2,6,6-tetramethylpiperidin-4-yl acrylate and bis(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate according to the general procedure of Example 2.
Sources & evidence
- ORD record
- ord-499b5ac854df49ec84f504b818b71439
- Source dataset
- uspto-grants-1991_05
- Patent number
- US05015678
Reaction notes
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