Reaktionsgleichung
[O:1]1[CH2:5][CH:4]=[CH:3][CH2:2]1.O.O[CH2:8][CH2:9][CH2:10][CH:11]=[O:12]>[Cr].[Co].O1CCCC1>[O:1]1[CH:2]=[CH:3][CH2:4][CH2:5]1.[O:12]1[CH:8]=[CH:9][CH:10]=[CH:11]1Komponenten
7
Edukt 3
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 120 °C
Versuchsvorschrift
A 300 ml stirred Hastelloy C autoclave was charged with 16 g 2,5-dihydrofuran, 80 g water and 5 g of the catalyst described in Example III. The autoclave was heated for 3 hours at 120° C. After cooling the resulting liquid was analysed by means of gas-liquid chromatography. The conversion of 2,5-dihydrofuran amounted to 55% gamma-hydroxy butyraldehyde having been formed with a selectivity of 65%. 2,3-Dihydrofuran, tetrahydrofuran and furan had also been formed in minor amounts.
Aufarbeitung
- temperatureAfter cooling the resulting liquid
- custombeen formed with a selectivity of 65%
Quellen und Nachweise
- ORD-Eintrag
- ord-2c2121915bee4d21b2d5558cff8b706c
- Quelldatensatz
- uspto-grants-1981_10
- Patentnummer
- US04297517
Verknüpfte Notizen
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