Reaktionsgleichung
[C:1]([O:7][CH3:8])(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4].C([N-]C(C)C)(C)C.[Li+].[CH:17](=[O:23])[CH:18]=[CH:19][CH:20]=[CH:21][CH3:22]>C1COCC1>[OH:4][CH:3]([CH2:5][C:17](=[O:23])[CH:18]=[CH:19][CH:20]=[CH:21][CH3:22])[CH2:2][C:1]([O:7][CH3:8])=[O:6]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- -78 °C
Versuchsvorschrift
To a cold (-30° C.) solution of methyl acetoacetate (41.5 g, 357 mmol) in THF (500 mL) was added lithium diisopropylamide (476 mL, 1.5M solution in cyclohexane, 714 mmol). The resultant solution was stirred for 15 minutes at -30° C. After cooling to -78° C., 2,4-hexadienal (34.3 g, 357 mmol) was added and the solution stirred for 10 minutes at -78° C. and for 16 hours at ambient temperature. The solution was concentrated under reduced pressure and the residual syrup was partitioned between 1N HCl and ethyl acetate. The organic layer was washed with brine (2x), dried (Na2SO4), and concentrated. The residue was purified by chromatography on silica gel (diethyl ether:hexane/2:1) to afford 18.5 g (24.4%) of the title compound as an oil.
Aufarbeitung
- concentrationThe solution was concentrated under reduced pressure
- customthe residual syrup was partitioned between 1N HCl and ethyl acetate
- washThe organic layer was washed with brine (2x)
- dry with materialdried (Na2SO4)
- concentrationconcentrated
- customThe residue was purified by chromatography on silica gel (diethyl ether:hexane/2:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-7a6eeb9a0b5d48cd86c76730c1eac551
- Quelldatensatz
- uspto-grants-1989_04
- Patentnummer
- US04824959
Verknüpfte Notizen
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