Reaktionsgleichung
[CH3:1][C:2]([CH3:13])([CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH3:12])[CH:7]=1)[CH2:3][OH:4]>O.[Rh]>[CH3:1][C:2]([CH3:13])([CH2:5][CH:6]1[CH2:11][CH2:10][CH2:9][CH:8]([CH3:12])[CH2:7]1)[CH2:3][OH:4]Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 60 °C
Versuchsvorschrift
5% Rh/C (450 mg, 15% w/w) was charged into a 50 mL autoclave vessel containing a mixture of 2,2-dimethyl-3-(3-methylphenyl)propan-1-ol (6 g, 34 mmol) in water (17 mL). The mixture was vigorously stirred under an hydrogen atmosphere (10 Bar) at 60° C. for 6 h. The reaction mixture was filtered and the filtrate was extracted with MTBE (25 mL), dried over magnesium sulphate and concentrated. The resulting crude product was distilled with a bulb-to-bulb distillation (2.5 mBar, 90° C.) to give 2,2-dimethyl-3-(3-methylcyclohexyl)propan-1-ol (5.1 g, gc purity>99%; yield 82%).
Aufarbeitung
- additioncontaining
- filtrationThe reaction mixture was filtered
- extractionthe filtrate was extracted with MTBE (25 mL)
- dry with materialdried over magnesium sulphate
- concentrationconcentrated
- distillationThe resulting crude product was distilled with a bulb-to-bulb distillation (2.5 mBar, 90° C.)
Quellen und Nachweise
- ORD-Eintrag
- ord-beb4fec26d5f494e9bee0fa0dfd974a8
- Quelldatensatz
- uspto-grants-2014_04
- Patentnummer
- US08709994B2
Verknüpfte Notizen
Wird geladen…