Reaktionsgleichung
Br[C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([F:9])[CH:3]=1.[C-:10]#[N:11].[Na+]>CN1CCCC1=O>[NH2:6][C:5]1[CH:7]=[CH:8][C:2]([C:10]#[N:11])=[CH:3][C:4]=1[F:9]Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
6.8 Parts of 4-bromo-2-fluoroaniline were dissolved in 75 parts of N-methylpyrrolidone. This solution was treated with 4.2 parts of cuprous cyanide. The reaction mixture was heated to 190° for 2 hours. The reaction mass was poured into a mixture of 200 parts of ice and 15 parts of sodium cyanide. This mixture was then heated on a steam bath for 2 hours at 60°-70°. This aqueous solution was then extracted with four 100-part portions of toluene. The toluene extracts were combined and washed with four 300-part portions of water followed by 100-parts of saturated aqueous NaCl. The toluene solution of the product was dried over sodium sulfate and evaporated at a reduced pressure of 50 mm.Hg to give 2.6 parts of 4-amino-3-fluorobenzonitrile, m.p. 71°-73°.
Aufarbeitung
- temperatureThe reaction mixture was heated to 190° for 2 hours
- temperatureThis mixture was then heated on a steam bath for 2 hours at 60°-70°
- extractionThis aqueous solution was then extracted with four 100-part portions of toluene
- washwashed with four 300-part portions of water
- dry with materialThe toluene solution of the product was dried over sodium sulfate
- customevaporated at a reduced pressure of 50 mm.Hg
Quellen und Nachweise
- ORD-Eintrag
- ord-bdb8f411cebd4de8940bc2439d415e08
- Quelldatensatz
- uspto-grants-1979_11
- Patentnummer
- US04175948
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