Reaktionsgleichung
[C:1]([OH:24])(=[O:23])[CH2:2][CH2:3][CH2:4]CCCCCCCC/C=C\CCCCCCCC.[CH:25](=[O:34])[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33].C(=[O:48])CCCCCCCCCCCC>>[C:1]([OH:24])(=[O:23])[CH2:2][CH2:3][CH2:4][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][C:25]([OH:48])=[O:34]Komponenten
4
Versuchsvorschrift
338.58 g (1 mol) of erucic acid (purity 95%) were ozonized in analogy to Example 1 and then hydrogenation was carried out. The hydrogenation solution obtained in this way contained nonanal and tridecanealdehyde acid and was divided by distillation. For oxidation, the corresponding aldehyde fraction was employed and was oxidized at 14 bar in analogy to Example 1. 185 g of tridecanedioic acid per cycle were obtained with a purity of 95%.
Aufarbeitung
- customThe hydrogenation solution obtained in this way
- distillationwas divided by distillation
Quellen und Nachweise
- ORD-Eintrag
- ord-1c2aa7fad9214de9be3b156d3fed97a7
- Quelldatensatz
- uspto-grants-1997_11
- Patentnummer
- US05686638
Verknüpfte Notizen
Wird geladen…