Bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidinyl)decandioate → HCID 53884686, compound

HRID 2051074Notes

Reaction equation

HRID 2051074 reaction equation
[C:1]([O:5][CH:6]1[CH2:11][C:10]([CH3:13])([CH3:12])[N:9]([O:14][CH3:15])[C:8]([CH3:17])([CH3:16])[CH2:7]1)(=[O:4])[CH:2]=[CH2:3].[C:18]([O:42][CH:43]1[CH2:48][C:47]([CH3:50])([CH3:49])[N:46]([OH:51])[C:45]([CH3:53])([CH3:52])[CH2:44]1)(=[O:41])[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][C:27]([O:29][CH:30]1[CH2:35][C:34]([CH3:37])([CH3:36])[N:33]([OH:38])[C:32]([CH3:40])([CH3:39])[CH2:31]1)=[O:28]>>[C:18]([O:42][CH:43]1[CH2:44][C:45]([CH3:53])([CH3:52])[N:46]([O:51][CH2:3][CH2:2][C:1]([O:5][CH:6]2[CH2:7][C:8]([CH3:16])([CH3:17])[N:9]([O:14][CH3:15])[C:10]([CH3:12])([CH3:13])[CH2:11]2)=[O:4])[C:47]([CH3:50])([CH3:49])[CH2:48]1)(=[O:41])[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][C:27]([O:29][CH:30]1[CH2:31][C:32]([CH3:39])([CH3:40])[N:33]([O:38][CH2:3][CH2:2][C:1]([O:5][CH:6]2[CH2:7][C:8]([CH3:17])([CH3:16])[N:9]([O:14][CH3:15])[C:10]([CH3:12])([CH3:13])[CH2:11]2)=[O:4])[C:34]([CH3:36])([CH3:37])[CH2:35]1)=[O:28]

Participants

3

Reactant 2

HCID 11272241Bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidinyl)decandioateHCID 19979416HCID 19979416, compound

Product 1

HCID 53884686HCID 53884686, compound

Procedure

The title compound is prepared from 1-methoxy-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-2701e1c2f1c347a484d463aa2c64023c
Source dataset
uspto-grants-1991_05
Patent number
US05015678

Reaction notes

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