Reaktionsgleichung
C([O:3][C:4](=[O:18])[CH:5]([CH:11]1[CH2:16][CH2:15][CH2:14][C:13](=[O:17])[CH2:12]1)C(OCC)=O)C.O=C1C(CCC)CCC(CC(O)=O)C1>>[O:17]=[C:13]1[CH2:14][CH2:15][CH2:16][CH:11]([CH2:5][C:4]([OH:18])=[O:3])[CH2:12]1Komponenten
3
Versuchsvorschrift
Step 2 (3-Oxo-cyclohexyl)-acetic acid was prepared in 70% yield from 2-(3-oxo-cyclohexyl)-malonic acid diethyl ester by the method described above for the synthesis of (3-oxo-4-propyl-cyclohexyl)-acetic acid: 1H NMR (300 MHz, CDCl3) δ 2.58–1.92 (m, 7H), 1.80–1.61 (m, 1H), 1.52–1.42 (m, 1H); ESI MS m/z 155 [M−H]−.
Quellen und Nachweise
- ORD-Eintrag
- ord-5cc29fa6b7524d0cbf47daa48a48fd93
- Quelldatensatz
- uspto-grants-2007_02
- Patentnummer
- US07176242B2
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