Reaktionsgleichung
[C:1]1(C)[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH:7]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[C:8]([OH:10])=[O:9].O=O.[C:30]([OH:33])(=[O:32])C>C([O-])(=O)C.[Co+2].C([O-])(=O)C>[C:30]([C:7]([C:2]1[CH:1]=[CH:6][CH:5]=[CH:4][CH:3]=1)([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[C:8]([OH:10])=[O:9])([OH:33])=[O:32]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 105 °C
Versuchsvorschrift
One-hundred and eight grams of the distilled tolylstearic acid was charged to a one-liter stirred Parr autoclave with 400 mls acetic acid and 50 gms cobalt (II) acetate. The reactor was sealed, heated to 105° C. and pressured with oxygen to 350 psig.
Aufarbeitung
- customThe reactor was sealed
Quellen und Nachweise
- ORD-Eintrag
- ord-9cb21e62965c4cd8bd3aea7918dbe682
- Quelldatensatz
- uspto-grants-1982_10
- Patentnummer
- US04356315
Verknüpfte Notizen
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