Reaktionsgleichung
[F:1][C:2]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:3]=1[CH2:4][NH2:5].[CH:11](=O)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.O>C1(C)C=CC=CC=1>[CH:11](=[N:5][CH2:4][C:3]1[CH:6]=[CH:7][C:8]([F:10])=[CH:9][C:2]=1[F:1])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
50.2 g (0.35 mol) of 2,4-difluorobenzylamine and 37.1 g (0.35 mol) of benzaldehyde are dissolved in 140 ml of toluene and heated to reflux. The water produced is separated off using a water separator. The reaction is complete (GC check) after two hours. The solution is evaporated on a vacuum rotary evaporator. 78.9 g (97% of theory) of a slightly yellow liquid are obtained.
Aufarbeitung
- temperatureheated to reflux
- customis separated off
- customafter two hours
- customThe solution is evaporated on a vacuum rotary evaporator
- custom78.9 g (97% of theory) of a slightly yellow liquid are obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-6267607942ce40488e1d03f6daa5f76d
- Quelldatensatz
- uspto-grants-1991_11
- Patentnummer
- US05068371
Verknüpfte Notizen
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