Water → HCID 86757237, Verbindung
Reaktionsgleichung
[Br-:1].[CH2:2]([N+:5]1([CH2:12][CH:13]=[CH2:14])[CH2:11][CH2:10][CH2:9][CH2:8]C[CH2:6]1)[CH:3]=[CH2:4].[Cl-:15].[CH2:16]([NH2+:19][CH2:20][CH:21]=[CH2:22])[CH:17]=[CH2:18].[OH2:23]>Cl.Cl.N(C(C(=N)N)(C)C)=NC(C(=N)N)(C)C>[Br-:1].[CH2:12]([N+:5]1([CH2:2][CH:3]=[CH2:4])[CH2:6][CH2:8][CH:9]([OH:23])[CH2:10][CH2:11]1)[CH:13]=[CH2:14].[Cl-:15].[CH2:16]([NH2+:19][CH2:20][CH:21]=[CH2:22])[CH:17]=[CH2:18]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 70 °C
Versuchsvorschrift
N,N-diallylhomopiperidinium bromide (13.0 g, EXAMPLE 4) and diallylammonium chloride (2.7 g, EXAMPLE 7) were dissolved in 15.0 g deionized water. To this aqueous solution was added 0.5 g of 2,2′-azobis(2-amidinopropane) dihydrochloride, the reaction mixture was bubbled with a slow stream of nitrogen gas for 45 minutes. While stirring, the temperature was raised to 70° C. The reaction mixture was stirred at 70° C. for 48 hours. After cooling to room temperature, 30.0 g of viscous polymer solution was obtained.
Aufarbeitung
- customthe reaction mixture was bubbled with a slow stream of nitrogen gas for 45 minutes
- stirringThe reaction mixture was stirred at 70° C. for 48 hours
- temperatureAfter cooling to room temperature
Quellen und Nachweise
- ORD-Eintrag
- ord-06da743b5b154aeab0135c3524fbeb69
- Quelldatensatz
- uspto-grants-2001_08
- Patentnummer
- US06271264B1
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