Furfuryl Alcohol → (5-((Diethylamino)methyl)furan-2-yl)methanol
Reaktionsgleichung
[CH:1]1[CH:5]=[C:4]([CH2:6][OH:7])[O:3][CH:2]=1.[CH2:8]([N:10]([CH2:17][CH3:18])[CH2:11]N(CC)CC)[CH3:9]>C(O)(=O)C>[CH2:8]([N:10]([CH2:11][C:2]1[O:3][C:4]([CH2:6][OH:7])=[CH:5][CH:1]=1)[CH2:17][CH3:18])[CH3:9]Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a solution of 2-furfuryl alcohol (8.24 g; 84 mmol) in 55 ml of acetic acid was added dropwise a solution of N,N,N',N'-tetraethyl-methylenediamine (20 g; 126 mmol)in 25 ml of acetic acid, and the solution was stirred at 0° C. for 30 minutes and at room temperature for 17 hours. The above solution was concentrated in vacuo, the residue was basified with dropwise addition of 30% of NaOH solution at 0° C. (to pH=11), and the mixture was extracted with ethyl acetate. The mixture was filtered, the organic layer was dried over sodium sulfate and concentrated in vacuo to yield a brown oil. The oil was distilled with a Kugelrohr Apparatus to afford 12.33 g (80%) of 5-diethylaminomethyl-2-hydroxymethylfuran as a yellow oil, b.p. 140° C./1 mm.
Aufarbeitung
- concentrationThe above solution was concentrated in vacuo
- additionthe residue was basified with dropwise addition of 30% of NaOH solution at 0° C. (to pH=11)
- extractionthe mixture was extracted with ethyl acetate
- filtrationThe mixture was filtered
- dry with materialthe organic layer was dried over sodium sulfate
- concentrationconcentrated in vacuo
- customto yield a brown oil
- distillationThe oil was distilled with a Kugelrohr Apparatus
Quellen und Nachweise
- ORD-Eintrag
- ord-bc68a41f0f0d466dbbcbe08d58efe4d9
- Quelldatensatz
- uspto-grants-1998_05
- Patentnummer
- US05750550
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