Reaktionsgleichung
[Cl-:1].[CH3:2][N+:3]([CH3:14])([CH3:13])[CH2:4][CH2:5][CH2:6][NH:7][C:8](=[O:12])[C:9]([CH3:11])=[CH2:10].[CH:15]([NH:18][C:19](=[O:22])[CH:20]=[CH2:21])([CH3:17])[CH3:16].[OH:23][CH2:24][CH2:25][O:26][C:27](=[O:31])[C:28]([CH3:30])=[CH2:29]>C(O)(C)C>[CH3:11][C:9]([C:8]([NH:7][CH2:6][CH2:5][CH2:4][N+:3]([CH3:14])([CH3:2])[CH3:13])=[O:12])=[CH2:10].[Cl-:1].[CH:15]([NH:18][C:19](=[O:22])[CH:20]=[CH2:21])([CH3:17])[CH3:16].[CH3:30][C:28]([C:27]([O:26][CH2:25][CH2:24][OH:23])=[O:31])=[CH2:29]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 75 °C
Versuchsvorschrift
To a 500 mL round-bottom, three-neck flask fitted with a thermocouple, reflux condenser, and septum was added 150 mL of isopropanol followed by 8.9 g of a 50% aqueous solution of N-(3-trimethylammoniopropyl)methacrylamide chloride, 15.3 g of N-iso-propylacrylamide, and 4.4 g of 2-hydroxyethylmethacrylate. The solution was purged with nitrogen for 1 hour and 0.5 g of AIBN was added. The mixture was purged for 15 min until all of the AIBN dissolved. The solution was heated to 75° C. under nitrogen for 16 hours.
Aufarbeitung
- customTo a 500 mL round-bottom, three-neck flask fitted with a thermocouple
- temperaturereflux condenser
- customThe solution was purged with nitrogen for 1 hour
- addition0.5 g of AIBN was added
- customThe mixture was purged for 15 min until all of the AIBN
- dissolutiondissolved
Quellen und Nachweise
- ORD-Eintrag
- ord-95ea9e826a8d42838452997224629e81
- Quelldatensatz
- uspto-grants-1999_12
- Patentnummer
- US06007803
Verknüpfte Notizen
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