Bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidinyl)decandioate → HCID 86744775, compound

HRID 2051073Notes

Reaction equation

HRID 2051073 reaction equation
C([O:5][CH:6]1[CH2:11][C:10]([CH3:13])([CH3:12])[N:9]([O:14][CH:15]2[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]2)[C:8]([CH3:22])([CH3:21])[CH2:7]1)(=O)C=C.[C:23]([O:47][CH:48]1[CH2:53][C:52]([CH3:55])([CH3:54])[N:51]([OH:56])[C:50]([CH3:58])([CH3:57])[CH2:49]1)(=[O:46])[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][C:32]([O:34][CH:35]1[CH2:40][C:39]([CH3:42])([CH3:41])[N:38]([OH:43])[C:37]([CH3:45])([CH3:44])[CH2:36]1)=[O:33]>>[C:23]([O:47][CH:48]1[CH2:49][C:50]([CH3:58])([CH3:57])[N:51]([O:56][CH2:17][C:16](=[C:15]=[O:14])[O:5][CH:6]2[CH2:11][C:10]([CH3:12])([CH3:13])[N:9]([O:14][CH:15]3[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]3)[C:8]([CH3:22])([CH3:21])[CH2:7]2)[C:52]([CH3:55])([CH3:54])[CH2:53]1)(=[O:46])[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][C:32]([O:34][CH:35]1[CH2:36][C:37]([CH3:44])([CH3:45])[N:38]([O:43][CH2:8][C:7](=[C:6]=[O:5])[O:5][CH:6]2[CH2:11][C:10]([CH3:12])([CH3:13])[N:9]([O:14][CH:15]3[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]3)[C:8]([CH3:21])([CH3:22])[CH2:7]2)[C:39]([CH3:41])([CH3:42])[CH2:40]1)=[O:33]

Participants

3

Reactant 2

HCID 11272241Bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidinyl)decandioateHCID 19979417HCID 19979417, compound

Product 1

HCID 86744775HCID 86744775, compound

Procedure

The title compound is prepared from 1-cyclohexyloxy-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-e7e23a63f6ce4d299e1110a72efcf23f
Source dataset
uspto-grants-1991_05
Patent number
US05015678

Reaction notes

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