Water → Cyclohexanol
Reaktionsgleichung
[CH:1]([O:3][CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1)=[O:2].O>CC(C)=O>[CH:1]([O:3][CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1)=[O:2].[CH:4]1([OH:3])[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1.[CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][CH:5]=1Komponenten
6
Edukt 2
Produkt 3
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1.29 g of cyclohexyl formate and 0.85 g of water were heated at 150° C. in an autoclave having a capacity of 25 mL, with stirring over a period of 2h. The pressure was 3.2 bar. The reaction mixture comprised two-phases both during and after the reaction. For analysis purposes, the two-phase effluent was homogenized with acetone. There were obtained, in addition to unconverted cyclohexyl formate, 6.5 mol %of cyclohexanol and 0.6 mol %of cyclohexene. Other by-products were not found. Quantitative analysis was carried out using GC (internal standard).
Aufarbeitung
- customafter the reaction
Quellen und Nachweise
- ORD-Eintrag
- ord-49e29e93bd0c45fa86ba5f0f4c5f4acb
- Quelldatensatz
- uspto-grants-1995_12
- Patentnummer
- US05475158
Notizen zur Reaktion
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