Reaktionsgleichung
[CH3:1][C:2](=[CH:4][CH2:5][CH2:6][C@H:7]([CH2:9][CH:10]=[O:11])[CH3:8])[CH3:3].C(=O)([O-])[O-].[Na+].[Na+].[H][H]>[Cr].[Cu]>[CH3:1][C:2](=[CH:4][CH2:5][CH2:6][C@@H:7]([CH2:9][CH2:10][OH:11])[CH3:8])[CH3:3]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Into a 100-ml autoclave were introduced 20.5 g (132.8 mmol) of (R)-citronellal, 1.0 g (5%, wt/wt) of a copper-chromium catalyst, and 0.04 g (0.2%, wt/wt) of sodium carbonate. After the atmosphere in the system was replaced with hydrogen, the reaction mixture was vigorously agitated in a hydrogen atmosphere (3.4 MPa) at 130° C. for 4.5 hours and then cooled. Thereafter, the catalyst was removed by filtration. The crude citronellol obtained was distilled under reduced pressure (70° C./1,870 Pa) to obtain 15.15 g of (S) -citronellol. Yield, 73%. Purity, 98.6% (of which α-citronellol accounted for 3.4%).
Aufarbeitung
- temperaturecooled
- customThereafter, the catalyst was removed by filtration
- customThe crude citronellol obtained
- distillationwas distilled under reduced pressure (70° C./1,870 Pa)
Quellen und Nachweise
- ORD-Eintrag
- ord-8854cd3a74a645768becf2b38a64d59e
- Quelldatensatz
- uspto-grants-2002_11
- Patentnummer
- US06486353B2
Verknüpfte Notizen
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