Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[F:11])[C:5]([NH2:7])=O.S(Cl)(Cl)=O>>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[F:11])[C:5]#[N:7]Komponenten
3
Versuchsvorschrift
765 g (3.5 moles) of 3-bromo-4-fluoro-benzoic acid amide was added, at 25° C., to 1,150 g (9.7 moles) of thionyl chloride and the mixture was heated under reflux at 85° to 90° C., while stirring, until virtually no further evolution of gas took place. The excess thionyl chloride was then distilled off and the residue was fractionated in a short column. 630 g (91% of theory) of 3-bromo-4-fluoro-benzonitrile with a boiling point of 115°-116° C./20 mm Hg were obtained.
Aufarbeitung
- temperaturethe mixture was heated
- temperatureunder reflux at 85° to 90° C.
- distillationThe excess thionyl chloride was then distilled off
Quellen und Nachweise
- ORD-Eintrag
- ord-389ca1d4043b4210994934deab942952
- Quelldatensatz
- uspto-grants-1983_05
- Patentnummer
- US04383949
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