4-Piperidinone, 2,2,6,6-tetramethyl-, oxime → HCID 22902710, compound

HRID 1654992Notes

Reaction equation

HRID 1654992 reaction equation
[CH3:1][C:2]1([CH3:12])[CH2:7][C:6](=[N:8][OH:9])[CH2:5][C:4]([CH3:11])([CH3:10])[NH:3]1.Br[CH2:14][C:15]1[CH:44]=[CH:43][C:18]([CH2:19][O:20][C:21](=[O:42])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][C:30]([O:32][CH2:33][C:34]2[CH:39]=[CH:38][C:37]([CH2:40]Br)=[CH:36][CH:35]=2)=[O:31])=[CH:17][CH:16]=1>>[CH3:1][C:2]1([CH3:12])[CH2:7][CH:6]([N:8]([CH2:14][C:15]2[CH:44]=[CH:43][C:18]([CH2:19][O:20][C:21](=[O:42])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][C:30]([O:32][CH2:33][C:34]3[CH:39]=[CH:38][C:37]([CH2:40][N:8]([CH:6]4[CH2:7][C:2]([CH3:12])([CH3:1])[NH:3][C:4]([CH3:11])([CH3:10])[CH2:5]4)[OH:9])=[CH:36][CH:35]=3)=[O:31])=[CH:17][CH:16]=2)[OH:9])[CH2:5][C:4]([CH3:11])([CH3:10])[NH:3]1

Participants

3

Procedure

from 2,2,6,6-tetramethylpiperidin-4-one oxime and di-(4-bromomethylbenzyl)sebacate

Sources & evidence

ORD record
ord-30258100ff9e4f1aafa81c6aae3af087
Source dataset
uspto-grants-1995_04
Patent number
US05410047

Reaction notes

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