1-Butanol → Butyl ether
Reaktionsgleichung
[CH2:1]([O:5][CH2:6][CH:7]=[CH:8][CH3:9])[CH2:2][CH2:3][CH3:4].[CH2:10]([OH:14])[CH2:11][CH2:12][CH3:13]>[Pd]>[CH2:6]([O:5][CH:1]([O:14][CH2:10][CH2:11][CH2:12][CH3:13])[CH2:2][CH2:3][CH3:4])[CH2:7][CH2:8][CH3:9].[CH2:1]([O:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH2:2][CH2:3][CH3:4].[CH2:6]([O:5][CH:1]=[CH:2][CH2:3][CH3:4])[CH2:7][CH2:8][CH3:9]Komponenten
6
Edukt 2
Produkt 3
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A glass autoclave was filled with 0.10 g of the heterogeneous catalyst palladium on active carbon (10% by weight of Pd), 3.0 g (24 mmol) of 1-butoxybut-2-ene and 1.73 g (24 mmol) of n-butanol. After 16 hours at 150° C. under a hydrogen atmosphere (1 bar), the reaction mixture was analyzed by means of calibrated gas chromatography. At a conversion of 21%, 1,1-dibutoxybutane was formed with a selectivity of 42%, dibutyl ether with a selectivity of 25% and 1-butoxybut-1-ene with a selectivity of 22%.
Quellen und Nachweise
- ORD-Eintrag
- ord-12afff5a5f0940d590b5fa135a0d5440
- Quelldatensatz
- uspto-grants-2000_12
- Patentnummer
- US06166265
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