Sodium Chloride → (E)-N-(2-(fluoromethylene)-4-(p-fluorophenyl)butyl)-N-formyl formamide
Reaktionsgleichung
[CH:1]([N-:3][CH:4]=[O:5])=[O:2].[Na+].C(#N)C.Cl[CH2:11]/[C:12](=[CH:22]/[F:23])/[CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=1.[Cl-].[Na+]>C1(C)C=CC=CC=1.O.CN(C)C=O>[F:23]/[CH:22]=[C:12](\[CH2:13][CH2:14][C:15]1[CH:16]=[CH:17][C:18]([F:21])=[CH:19][CH:20]=1)/[CH2:11][N:3]([CH:4]=[O:5])[CH:1]=[O:2]Komponenten
8
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
Combine sodium diformylamide (70 lb) and acetonitrile (903 lb). With agitation, add N,N-dimethylformamide (119 lb). Add a solution of (E)-1-chloro-2-(fluoromethylene)-4-(p-fluorophenyl)butane (126 lb) in toluene. Warm to 80° C. After 6 hours, add a 10% by weight solution of sodium chloride in water (1168 lb). Agitate for 15 minutes, separate the layers. Remove the organic layer to give the title compound as a solution in acetonitrile/N,N-dimethylformamide.
Aufarbeitung
- customseparate the layers
- customRemove the organic layer
Quellen und Nachweise
- ORD-Eintrag
- ord-73fdb5f652bb47e49c7344d800ba6cbc
- Quelldatensatz
- uspto-grants-1997_02
- Patentnummer
- US05599986
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