Reaktionsgleichung
[CH3:1][C@@:2]12[CH:10](C(C([O-])=O)=C)[CH2:9][C@H:5]([C:6]1([CH3:8])[CH3:7])[CH2:4][CH2:3]2.[C:16]([O:20][CH3:21])(=[O:19])[CH:17]=[CH2:18].[C:22]([OH:26])(=[O:25])[CH:23]=[CH2:24].CCCCCCCCCC(C)C.C(C(CCCC)C(OOC(C)(CCC(OOC(=O)C(CC)CCCC)(C)C)C)=O)C>>[C:16]([O:20][CH:10]1[CH2:9][CH:5]2[C:6]([CH3:7])([CH3:8])[C:2]1([CH3:1])[CH2:3][CH2:4]2)(=[O:19])[CH:17]=[CH2:18].[C:22]([OH:26])(=[O:25])[CH:23]=[CH2:24].[C:16]([O:20][CH3:21])(=[O:19])[CH:17]=[CH2:18]Komponenten
6
Versuchsvorschrift
18 g of isobornyl acrylate, 71.1 g of methyl acrylate, 0.9 g of acrylic acid, 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 1 hour.
Quellen und Nachweise
- ORD-Eintrag
- ord-c274811ea69a4421b120c4eee40bee57
- Quelldatensatz
- uspto-grants-2010_09
- Patentnummer
- US07803877B2
Verknüpfte Notizen
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