Ethyl chloroformate → N-ethoxycarbonyl-bis(2,2,6,6-tetramethyl-4-piperidyl)-amine

HRID 1248657Notes

Reaction equation

HRID 1248657 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

  1. customat 10°-20° C.
  2. customThe product obtained

Sources & evidence

ORD record
ord-68566f806ccd4cdfb55018c5f4361d16
Source dataset
uspto-grants-1985_06
Patent number
US04525503

Reaction notes

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