Reaktionsgleichung
[C:1]([O:5][CH2:6][CH:7]([CH3:9])[CH3:8])(=[O:4])[CH:2]=[CH2:3].CCC[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH:19]([CH3:21])[CH3:20].[CH2:22]([CH:24]([CH2:48]CCC)[C:25]([O:27]OC(C)(CCC(O[O:37][C:38](=[O:46])[CH:39]([CH2:44]C)[CH2:40]CCC)(C)C)C)=[O:26])C>>[CH3:48][C:24]([C:25]([O:27][CH:16]1[C@@:15]2([CH3:1])[C:19]([CH3:20])([CH3:21])[C@H:18]([CH2:13][CH2:14]2)[CH2:17]1)=[O:26])=[CH2:22].[C:38]([O:37][CH2:6][CH:7]([CH3:9])[CH3:8])(=[O:46])[C:39]([CH3:40])=[CH2:44].[C:1]([O:5][CH2:6][CH:7]([CH3:9])[CH3:8])(=[O:4])[CH:2]=[CH2:3]Komponenten
4
Versuchsvorschrift
90 g of isobutyl acrylate, 90 g of isododecane and 1.2 g of 2,5-bis(2-ethylhexanoylperoxy)-2,5-dimethylhexane were then introduced into the above mixture, still at 90° C. and over 30 minutes.
Quellen und Nachweise
- ORD-Eintrag
- ord-3c0732d14b754aabb9e9c20b0ea03829
- Quelldatensatz
- uspto-grants-2011_03
- Patentnummer
- US07915347B2
Verknüpfte Notizen
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