Ethyl chloroformate → N-ethoxycarbonyl-bis(2,2,6,6-tetramethyl-4-piperidyl)-amine
Reaction equation
[CH3:1][C:2]1([CH3:21])[CH2:7][CH:6]([NH:8][CH:9]2[CH2:14][C:13]([CH3:16])([CH3:15])[NH:12][C:11]([CH3:18])([CH3:17])[CH2:10]2)[CH2:5][C:4]([CH3:20])([CH3:19])[NH:3]1.[C:22](Cl)(=[O:26])[O:23][CH2:24][CH3:25].[OH-].[Na+]>C(Cl)(Cl)Cl>[CH2:24]([O:23][C:22]([N:8]([CH:9]1[CH2:14][C:13]([CH3:16])([CH3:15])[NH:12][C:11]([CH3:18])([CH3:17])[CH2:10]1)[CH:6]1[CH2:7][C:2]([CH3:21])([CH3:1])[NH:3][C:4]([CH3:20])([CH3:19])[CH2:5]1)=[O:26])[CH3:25]Participants
5
Procedure
The N-ethoxycarbonyl-bis(2,2,6,6-tetramethyl-4-piperidyl)-amine is prepared by reacting bis(2,2,6,6-tetramethyl-4-piperidyl)-amine with ethyl chlorocarbonate in chloroform at 10°-20° C. in the presence of aqueous NaOH. The product obtained, which has a purity of 99.2% and melts at 117° C., can be used directly.
Workup
- customat 10°-20° C.
- customThe product obtained
Sources & evidence
- ORD record
- ord-3ad9167f62ec490ba33722290a226711
- Source dataset
- uspto-grants-1983_01
- Patent number
- US04369321
Reaction notes
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