Reaktionsgleichung
[C:1](O)(=[O:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[O:10]1[CH:14]=[CH:13][CH:12]=[CH:11]1.ClC(Cl)C(OC(=O)C(Cl)Cl)=O.[B]>C1(C)C=CC=CC=1>[C:1]([C:11]1[O:10][CH:14]=[CH:13][CH:12]=1)(=[O:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 50 °C
Versuchsvorschrift
In 50 ml of toluene were dissolved 6.51 g (0.05 mole) of heptanoic acid, 4.43 g (0.065 mole) of furan and 14.39 g (0.06 mole) of dichloroacetic anhydride. To the resulting solution was added 0.71 g of boron trifluoridediethyl ether coplex and the resulting mixture was then stirred at 50° C. for 3 hours. After completion of the reaction, the reaction solution was cooled and washed successively with 5% aqueous sodium carbonate solution and water. The organic layer was concentrated under reduced pressure and the resulting concentrated residue was then purified by silica gel-filled column chromatography to obtain 8.95 g of 2-heptanoylfuran.
Aufarbeitung
- customAfter completion of the reaction
- temperaturethe reaction solution was cooled
- washwashed successively with 5% aqueous sodium carbonate solution and water
- concentrationThe organic layer was concentrated under reduced pressure
- customthe resulting concentrated residue was then purified by silica gel-
- additionfilled column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-218971747ed74ae7872997c922fec91f
- Quelldatensatz
- uspto-grants-1989_03
- Patentnummer
- US04812585
Verknüpfte Notizen
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