Tridecanal → Tridecanedioic acid

HRID 2293814

Reaktionsgleichung

Reaktionsgleichung von HRID 2293814
[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

  1. customThe hydrogenation solution obtained in this way
  2. distillationwas divided by distillation

Quellen und Nachweise

ORD-Eintrag
ord-1c2aa7fad9214de9be3b156d3fed97a7
Quelldatensatz
uspto-grants-1997_11
Patentnummer
US05686638

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