Cyclohexanone → 2-(3-oxo-3-phenylpropyl)cyclohexanone
Reaktionsgleichung
CN(C)[CH2:3][CH2:4][C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:6].[C:14]1(=[O:20])[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1>>[C:7]1([C:5](=[O:6])[CH2:4][CH2:3][CH:15]2[CH2:16][CH2:17][CH2:18][CH2:19][C:14]2=[O:20])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1Komponenten
Versuchsvorschrift
2-(3'-Phenyl-3'-oxopropyl)cyclohexanone was prepared accordinf to the method of W. Hahn and J. Epsztain (Roozniki Chem. 1963, 37, 403-12): A mixture of β-dimethylaminopropiophenone (27 gm.) and cyclohexanone (37.5 g.) were heated at reflux for 5 hours under nitrogen and the solvent removed in vacuo. The residual oil was distilled giving 2-(3'-phenyl-3'-oxopropyl)cyclohexanone (14 g.) which was cyclised to the title compound according to the method of Hahn and Epsztain by dissolving the diketone (12 g.) in ethanol (65 ml.), treating with hydroxylamine hydrochloride (9 g.) and heating under reflux for 1 hour. The cooled reaction mixture was poured onto water (300 ml.), extracted with ether (2 × 50 ml.) and the extracts discarded. The aqueous solution was made basic with K2CO3 and extracted with ether (3 × 50 ml.). The combined ether extracts were dried and the solvent removed in vacuo. The residual oil was distilled to give the title compound as a colourless oil (7 g.) b.p. 134°-8° C/15 mm. Found: C, 85.40; H.7.5; N, 6.9%, C15H15N requires: C, 86.00; H, 7.2; N, 6.7%
Aufarbeitung
- custom2-(3'-Phenyl-3'-oxopropyl)cyclohexanone was prepared accordinf to the method of W
- temperaturewere heated
- temperatureat reflux for 5 hours under nitrogen
- customthe solvent removed in vacuo
- distillationThe residual oil was distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-9b3b78283cfe48ebb478d68c64f9fc98
- Quelldatensatz
- uspto-grants-1977_06
- Patentnummer
- US04031102
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