Cyanuric chloride → HCID 21182127, compound
Reaction equation
[CH3:1][O:2][N:3]1[C:8]([CH3:10])([CH3:9])[CH2:7][CH:6]([CH2:11][CH2:12][CH2:13][CH2:14][NH2:15])[CH2:5][C:4]1([CH3:17])[CH3:16].[N:18]1[C:25]([Cl:26])=[N:24][C:22](Cl)=[N:21][C:19]=1[Cl:20].[OH-].[Na+]>C1(C)C(C)=CC=CC=1.O>[Cl:20][C:19]1[N:18]=[C:25]([Cl:26])[N:24]=[C:22]([NH:15][CH2:14][CH2:13][CH2:12][CH2:11][CH:6]2[CH2:7][C:8]([CH3:10])([CH3:9])[N:3]([O:2][CH3:1])[C:4]([CH3:17])([CH3:16])[CH2:5]2)[N:21]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
39.7 g (163 mmoles) of N-(1-methoxy-2,2,6,6-tetramethyl-4-piperidyl)butylamine are slowly added to a solution of 30 g (163 mmoles) of cyanuric chloride in 180 ml of xylene, maintained at room temperature. After the addition, the mixture is stirred for ½ hour at room temperature and subsequently, a solution of 6.8 g (170 mmoles) of sodium hydroxide in 45 ml of water is slowly added, maintaining the temperature at room temperature.
Workup
- additionAfter the addition
- temperaturemaintaining the temperature at room temperature
Sources & evidence
- ORD record
- ord-2bcdd30447704c26926d40e0c6b8bf2b
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06265473B1
Reaction notes
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