Reaktionsgleichung
[CH:1]12[CH2:7][CH:4]([CH2:5][CH2:6]1)[CH:3]=[CH:2]2.[CH:8]12[CH2:14][CH:11]([CH:12]=[CH:13]1)[CH2:10][CH:9]2[CH2:15][OH:16].[CH:17]12[CH2:23][CH:20]([CH:21]=[CH:22]1)[CH2:19][CH:18]2[C:24]([OH:26])=[O:25].[C:27]1(=[O:33])[O:32][C:30](=[O:31])[CH:29]=[CH:28]1.CC(N=NC(C#N)(C)C)(C#N)C>O1CCCC1>[CH:8]12[CH2:14][CH:11]([CH:12]=[CH:13]1)[CH2:10][CH:9]2[CH2:15][OH:16].[CH:17]12[CH2:23][CH:20]([CH:21]=[CH:22]1)[CH2:19][CH:18]2[C:24]([OH:26])=[O:25].[CH:1]12[CH2:7][CH:4]([CH2:5][CH2:6]1)[CH:3]=[CH:2]2.[C:30]1(=[O:31])[O:32][C:27](=[O:33])[CH:28]=[CH:29]1Komponenten
7
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 70 ml of tetrahydrofuran was added 0.04 M of norbornylene, 0.1 M of bicyclo[2.2.1]hept-5-ene-2-methanol, 0.06 M of bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 0.2 M of maleic anhydride and 0.4 g of AIBN. The resulting solution was reacted at 67° C. for 8 hours. Thereafter, a polymer was precipitated and filtered in petroleum ether/ether (1/1) solution, to obtain the title polymer. Here, the polymer was washed with aqueous Na2CO3 solution (5%), and re-washed with distilled water to completely remove base. The resulting resin was vacuum-dried to obtain a pure resin (yield: 51%).
Aufarbeitung
- customThe resulting solution was reacted at 67° C. for 8 hours
- customThereafter, a polymer was precipitated
- filtrationfiltered in petroleum ether/ether (1/1) solution
Quellen und Nachweise
- ORD-Eintrag
- ord-3da923555ce94d79bc6c6fa0db87a994
- Quelldatensatz
- uspto-grants-2003_10
- Patentnummer
- US06630281B2
Verknüpfte Notizen
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