Reaktionsgleichung
[CH3:1][CH:2]([CH2:26][CH2:27][CH:28]=[C:29]([CH3:31])[CH3:30])[CH2:3][CH2:4][O:5][C:6](=[O:25])[CH2:7][CH2:8][CH2:9][CH2:10]CCCCCC[Si](C)(C)O[Si](C)(C)C.CC(CCC=C(C)C)CCOC(=O)CCCCCCCCC=C.[CH3:55][SiH:56]([CH3:62])[O:57][Si:58]([CH3:61])([CH3:60])[CH3:59]>>[CH3:1][CH:2]([CH2:26][CH2:27][CH:28]=[C:29]([CH3:30])[CH3:31])[CH2:3][CH2:4][O:5][C:6](=[O:25])[CH2:7][CH2:8][CH2:9][CH2:10][Si:56]([CH3:62])([CH3:55])[O:57][Si:58]([CH3:61])([CH3:60])[CH3:59]Komponenten
4
Edukt 3
Produkt 1
Versuchsvorschrift
According to the same procedure, 11-(1,1,3,3,3-pentamethyl-disiloxanyl)-undecanoic acid 3,7-dimethyl-oct-6-enyl ester was prepared from undec-10-enoic acid 3,7-dimethyl-oct-6-enyl ester and pentamethyldisiloxane.
Quellen und Nachweise
- ORD-Eintrag
- ord-5217759710784b679c9b29671c05a691
- Quelldatensatz
- uspto-grants-2001_07
- Patentnummer
- US06262287B1
Verknüpfte Notizen
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