Cyanuric chloride → HCID 19832518, compound

HRID 2051580Notes

Reaction equation

HRID 2051580 reaction equation
[OH:1][CH:2]1[CH2:7][C:6]([CH3:9])([CH3:8])[N:5]([O:10][CH3:11])[C:4]([CH3:13])([CH3:12])[CH2:3]1.[H-].[Na+].[N:16]1[C:23](Cl)=[N:22][C:20](Cl)=[N:19][C:17]=1Cl>O1CCOCC1>[CH3:11][O:10][N:5]1[C:6]([CH3:8])([CH3:9])[CH2:7][CH:2]([O:1][C:17]2[N:19]=[C:20]([O:1][CH:2]3[CH2:7][C:6]([CH3:8])([CH3:9])[N:5]([O:10][CH3:11])[C:4]([CH3:13])([CH3:12])[CH2:3]3)[N:22]=[C:23]([O:1][CH:2]3[CH2:7][C:6]([CH3:8])([CH3:9])[N:5]([O:10][CH3:11])[C:4]([CH3:13])([CH3:12])[CH2:3]3)[N:16]=2)[CH2:3][C:4]1([CH3:13])[CH3:12]

Participants

5

Reactant 3

HCID 7954Cyanuric chlorideHCID 24758Sodium hydrideHCID 109977701-Methoxy-2,2,6,6-tetramethyl-piperidin-4-ol

Product 1

HCID 19832518HCID 19832518, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

The title compound is prepared by the reaction of 4-hydroxy-1-methoxy-2,2,6,6-tetramethylpiperidine, sodium hydride, and cyanuric chloride in 1,4-dioxane solvent.

Sources & evidence

ORD record
ord-37f6b190af2142bbbc556b4c6c5c8e4a
Source dataset
uspto-grants-1991_05
Patent number
US05019613

Reaction notes

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