Reaktionsgleichung
[C:1]([O:6][C:7]1([CH2:17][CH3:18])[CH:14]2[CH2:15][CH:10]3[CH2:11][CH:12]([CH2:16][CH:8]1[CH2:9]3)[CH2:13]2)(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:19]([O:22][C:23]1[CH:30]=[CH:29][C:26]([CH:27]=[CH2:28])=[CH:25][CH:24]=1)(=[O:21])[CH3:20].N(C(C)(C)C(OC)=O)=NC(C)(C)C(OC)=O.CO>C(O)(C)C.CC(C)=O>[C:1]([O:6][C:7]1([CH2:17][CH3:18])[CH:8]2[CH2:16][CH:12]3[CH2:11][CH:10]([CH2:15][CH:14]1[CH2:13]3)[CH2:9]2)(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:19]([O:22][C:23]1[CH:30]=[CH:29][C:26]([CH:27]=[CH2:28])=[CH:25][CH:24]=1)(=[O:21])[CH3:20]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 75 °C
Versuchsvorschrift
Into a flask were added 39.7 g (0.16 mol) of 2-ethyl-2-adamantyl methacrylate, 103.8 g (0.64 mol) of p-acetoxystyrene and 265 g of isopropanol, followed by heating up to 75° C. under an atmosphere of nitrogen. To this solution was dropped a solution of 11.05 g (0.048 mol) of dimethyl 2,2′-azobis(2-methylpropionate) dissolved in 22.11 g of isopropanol. The solution was heated for about 0.3 hour at 75° C. and further refluxed for about 12 hours. After diluting with acetone, the reaction mixture was poured into a large amount of methanol to precipitate the polymerized product, which was separated by filtration. The weight of the obtained copolymer of 2-ethyl-2-adamantyl methacrylate and p-acetoxystyrene was 250 g (note: wet weight of cake containing methanol).
Aufarbeitung
- temperatureThe solution was heated for about 0.3 hour at 75° C.
- temperaturefurther refluxed for about 12 hours
- customto precipitate the polymerized product, which
- customwas separated by filtration
- addition250 g (note: wet weight of cake containing methanol)
Quellen und Nachweise
- ORD-Eintrag
- ord-ea5570b322b1480a91ecb70cd53397da
- Quelldatensatz
- uspto-grants-2005_05
- Patentnummer
- US06893794B2
Verknüpfte Notizen
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