Reaktionsgleichung
[C:1]([O:4][CH:5]([CH3:8])[CH:6]=O)(=O)[CH3:2].[C:9]([O:15][CH3:16])(=[O:14])[CH2:10]C(C)=O>[Fe].CO>[CH3:16][O:15][C:9]([C:10]1[CH:6]=[C:5]([CH3:8])[O:4][C:1]=1[CH3:2])=[O:14]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
40 parts by weight of iron-III chloride and 136 parts by weight of 85 percent strength α-acetoxypropionaldehyde are added successively to a solution of 150 parts by weight of methyl acetoacetate in 120 parts by weight of methanol. The mixture, which becomes warm, is then refluxed for 2 hours. When it has cooled, the reaction solution is washed with water and distilled. 127 g of 2,5-dimethylfuran-3-carboxylic acid methyl ester are obtained.
Aufarbeitung
- temperatureThe mixture, which becomes warm
- temperatureis then refluxed for 2 hours
- temperatureWhen it has cooled
- washthe reaction solution is washed with water
- distillationdistilled
Quellen und Nachweise
- ORD-Eintrag
- ord-a86d7762caed427391b66ee59855b844
- Quelldatensatz
- uspto-grants-1980_06
- Patentnummer
- US04207243
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