Reaktionsgleichung
[CH:1]1[C:6]([NH2:7])=[CH:5][CH:4]=[C:3]([OH:8])[CH:2]=1.Cl[C:10]([F:14])([F:13])[CH2:11][Cl:12].C([O-])([O-])=O.[K+].[K+].C(#N)C>O>[Cl:12][CH2:11][C:10]([F:14])([F:13])[O:8][C:3]1[CH:4]=[CH:5][C:6]([NH2:7])=[CH:1][CH:2]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2.5 g (22.9 mmol) of p-aminophenol, 3.09 g (22.9 mmol) of 1,2-dichloro-1,1-difluoroethane, 5.48 g (39.6 mmol) of K2CO3 and 40 ml of dry acetonitrile were stirred together at room temperature for 5 days. The mixture was poured into water and extracted two times into ether. The combined ether extracts were washed with water, dried over MgSO4 and filtered: HCl gas was bubbled into the ether solution causing the above-named aniline to precipitate as the hydrochloride salt, which was collected by filtration and recrystallized twice from CH3CN to give 0.9 g (16 percent of theoretical d 245°-250° C.) of a white solid.
Aufarbeitung
- extractionextracted two times into ether
- washThe combined ether extracts were washed with water
- dry with materialdried over MgSO4
- filtrationfiltered
- customHCl gas was bubbled into the ether solution
- customto precipitate as the hydrochloride salt, which
- filtrationwas collected by filtration
- customrecrystallized twice from CH3CN
- customto give 0.9 g (16 percent of theoretical d 245°-250° C.) of a white solid
Quellen und Nachweise
- ORD-Eintrag
- ord-c511a8c8feb8478d9e51ff3b4f62f5c5
- Quelldatensatz
- uspto-grants-1993_10
- Patentnummer
- US05250690
Verknüpfte Notizen
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