Methyl 3-(2,4-dimethoxy-5-propionylphenyl)octanoate → 3-(2,4-Dimethoxy-5-propionylphenyl)octanoic acid
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[C:6]([C:11](=[O:14])[CH2:12][CH3:13])=[CH:5][C:4]=1[CH:15]([CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[CH2:16][C:17]([O:19]C)=[O:18]>C(OCC)(=O)C.CCCCCC>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[C:6]([C:11](=[O:14])[CH2:12][CH3:13])=[CH:5][C:4]=1[CH:15]([CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[CH2:16][C:17]([OH:19])=[O:18]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The methyl 3-(2,4-dimethoxy-5-propionylphenyl)octanoate prepared as described in step (i) above was hydrolyzed in a similar manner to that described in Preparation 7 to give the title compound as crystals, melting at 92.5-94° C. (from ethyl acetate-hexane).
Aufarbeitung
- customdescribed in Preparation 7
Quellen und Nachweise
- ORD-Eintrag
- ord-0c6227b3ebe64d149980d08a1d0f32c0
- Quelldatensatz
- uspto-grants-2000_03
- Patentnummer
- US06040339
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