Reaktionsgleichung
[OH:1][CH2:2]/[CH:3]=[C:4](/[CH3:11])\[CH2:5][CH2:6][CH:7]=[C:8]([CH3:10])[CH3:9].[H][H]>C1C=CC=CC=1>[CH3:9][C:8](=[CH:7][CH2:6][CH2:5][C@@H:4]([CH2:3][CH2:2][OH:1])[CH3:11])[CH3:10]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In a 100 ml stainless steel-made autoclave whose atmosphere had been displaced with nitrogen were charged 1.54 g (10 mmole) of nerol, 0.0837 g (0.1 mmole) of Rh(COD)((+)-cBINAP)Cl obtained in Example 4, and 10 ml of benzene, and hydrogenation reaction was carried out at room temperature and at a hydrogen pressure of 30 kg/cm2 for 17 hours. There was obtained 1.46 g of (S)-(-)-citronellol at a conversion of 99% and a selectivity of 99%. From the results of optical rotation [α]25D =-3.65° (c=10.1, chloroform), the optical yield was found to be 70%ee.
Aufarbeitung
- additionwere charged
Quellen und Nachweise
- ORD-Eintrag
- ord-40c1ffd65a72440ca4c4af287452b7d2
- Quelldatensatz
- uspto-grants-1994_05
- Patentnummer
- US05312939
Verknüpfte Notizen
Wird geladen…