Reaktionsgleichung
[C:1]([O:5][C:6](=[O:9])[CH:7]=[CH2:8])([CH3:4])([CH3:3])[CH3:2].[C:10]([NH2:14])(=[O:13])[CH:11]=[CH2:12]>C(O)(C)C>[C:1]([O:5][C:6](=[O:9])[CH:7]=[CH2:8])([CH3:4])([CH3:3])[CH3:2].[C:10]([NH2:14])(=[O:13])[CH:11]=[CH2:12]Komponenten
4
Edukt 2
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 16.13 g of a 50% aqueous solution of 2-trimethylammoniumethylacrylate chloride, 8.06 g of t-butylacrylate, and 8.06 g of acrylarnide. The solution was purged with nitrogen for 1 hour and 0.5 g AIBN was added. The mixture was purged for ˜15 minutes 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 AIBN was added
- customThe mixture was purged for ˜15 minutes until all of the AIBN
- dissolutiondissolved
Quellen und Nachweise
- ORD-Eintrag
- ord-941bf5340a6a4b8692547611eed49250
- Quelldatensatz
- uspto-grants-2002_05
- Patentnummer
- US06395777B2
Verknüpfte Notizen
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