1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine → HCID 67827820, compound
Reaction equation
[C:1](Cl)(=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10](Cl)=[O:11].[OH:15][CH:16]1[CH2:21][C:20]([CH3:23])([CH3:22])[N:19]([O:24][CH3:25])[C:18]([CH3:27])([CH3:26])[CH2:17]1.[OH:28][CH:29]1[CH2:34][C:33]([CH3:36])([CH3:35])[N:32]([OH:37])[C:31]([CH3:39])([CH3:38])[CH2:30]1.C(N(CC)CC)C>C(Cl)Cl>[C:1]([O:15][CH:16]1[CH2:21][C:20]([CH3:22])([CH3:23])[N:19]([O:24][CH3:25])[C:18]([CH3:27])([CH3:26])[CH2:17]1)(=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:28][CH:29]1[CH2:34][C:33]([CH3:35])([CH3:36])[N:32]([OH:37])[C:31]([CH3:39])([CH3:38])[CH2:30]1)=[O:11]Participants
6
Procedure
Sebacoyl chloride is added to a mixture of 4-hydroxy-1-methoxy-2,2,6,6-tetramethylpiperidine, 4-hydroxyl-1-oxyl-2,2,6,6-tetramethylpiperidine, triethylamine and methylene chloride. The reaction mixture is worked up in the usual manner and purified by flash chromatography on silica gel to afford the title compound.
Workup
- custompurified by flash chromatography on silica gel
Sources & evidence
- ORD record
- ord-2a179d901f994219952c061a6d4bc8d7
- Source dataset
- uspto-grants-1991_05
- Patent number
- US05015682
Reaction notes
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