Cyanuric chloride → HCID 21468019, Verbindung

HRID 1681439Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1681439
[CH3:1][C:2]1([CH3:28])[CH2:7][CH:6]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][CH:16]2[CH2:21][C:20]([CH3:23])([CH3:22])[NH:19][C:18]([CH3:25])([CH3:24])[CH2:17]2)[CH2:5][C:4]([CH3:27])([CH3:26])[NH:3]1.[N:29]1[C:36]([Cl:37])=[N:35][C:33]([Cl:34])=[N:32][C:30]=1Cl.[OH-].[Na+]>ClCCCl>[Cl:34][C:33]1[N:35]=[C:36]([Cl:37])[N:29]=[C:30]([N:8]([CH:6]2[CH2:7][C:2]([CH3:28])([CH3:1])[NH:3][C:4]([CH3:27])([CH3:26])[CH2:5]2)[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][N:15]([C:30]2[N:29]=[C:36]([Cl:37])[N:35]=[C:33]([Cl:34])[N:32]=2)[CH:16]2[CH2:17][C:18]([CH3:25])([CH3:24])[NH:19][C:20]([CH3:23])([CH3:22])[CH2:21]2)[N:32]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution of 118.20 g (0.30 mol) of N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-diaminohexane in 150 ml of 1,2-dichloroethane is added slowly in the course of 2 hours to a solution, maintained at 0° C., containing 110.70 g (0.60 mol) of cyanuric chloride in 800 ml of 1,2-dichloroethane. 250 ml of an aqueous solution containing 25.20 g (0.63 mol) of sodium hydroxide are then added in 30 minutes at 0° C., and stirring is continued for 2 hours at 0° C. The aqueous phase is then separated off, the organic phase is washed repeatedly with water and dehydrated by means of anhydrous sodium sulfate, and a white solid of melting point 161°-163° C. is precipitated by evaporation of the solvent.

Aufarbeitung

  1. additionare then added in 30 minutes at 0° C.
  2. customThe aqueous phase is then separated off
  3. washthe organic phase is washed repeatedly with water and dehydrated by means of anhydrous sodium sulfate
  4. customa white solid of melting point 161°-163° C. is precipitated by evaporation of the solvent

Quellen und Nachweise

ORD-Eintrag
ord-ae92da7bd089424688e12961289f0605
Quelldatensatz
uspto-grants-1992_12
Patentnummer
US05171855

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