Reaktionsgleichung
C1CCCCCCC=1.ON1[C:14](=O)[C:13]2=[CH:16][CH:17]=[CH:18][CH:19]=[C:12]2[C:11]1=[O:20].O=O>C(#N)C>[C:11]1(=[O:20])[CH2:14][CH2:13][CH2:16][CH2:17][CH2:18][CH:19]=[CH:12]1.[CH:11]1([OH:20])[CH2:14][CH2:13][CH2:16][CH2:17][CH2:18][CH:19]=[CH:12]1Komponenten
6
Edukt 3
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 1.10 grams (10 millimoles) of cyclooctene, 0.13 gram (0.8 millimole) of N-hydroxyphthalimide, 0.021 gram (0.06 millimole) of acetylacetonatocobalt Co(AA)2 and 25 milliliters of acetonitrile was stirred in an oxygen atmosphere at a temperature of 100° C. for 6 hours. The product in the reaction mixture was analyzed with gas chromatography. Cyclooctene was transformed, with a transformation rate of 95%, into 2-cycloocten-1-one (cyclooctene-based selectivity 82%, yield 78%) and 2-cycloocten-1-ol (cyclooctene-based selectivity 16%, yield 15%).
Quellen und Nachweise
- ORD-Eintrag
- ord-5629545e6ea04bcdaa5d4c52c2efc6e4
- Quelldatensatz
- uspto-grants-1999_09
- Patentnummer
- US05958821
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