2-Propylpent-4-enal → 2-Propylpentanal
Reaktionsgleichung
[CH2:1]([CH:4]([CH2:7][CH:8]=[CH2:9])[CH:5]=[O:6])[CH2:2][CH3:3].[H][H]>[Pd].C(OCC)(=O)C>[CH2:1]([CH:4]([CH2:7][CH2:8][CH3:9])[CH:5]=[O:6])[CH2:2][CH3:3]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A Parr hydrogenation bottle was charged with 10% palladium on carbon (0.1 equivalent) and ethyl acetate. A solution of 2-propylpent 4 enal, prepared as in Example 5, in ethyl acetate was added. The mixture was hydrogenated at 300N/m2 hydrogen in a Parr hydrogenation apparatus at room temperature until hydrogen uptake ceased. The catalyst was removed by filtration through celite. The filtrate was concentrated to give the desired product as a colorless oil. The product was used without further purification.
Aufarbeitung
- customThe catalyst was removed by filtration through celite
- concentrationThe filtrate was concentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-346b3ce8d2ff4b18a02f7558503cc7fe
- Quelldatensatz
- uspto-grants-1990_10
- Patentnummer
- US04963557
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