Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH3:9].F[B-](F)(F)F.[O:15]=[N+:16]=[O:17]>ClCCl>[Br:1][C:2]1[CH:7]=[C:6]([N+:16]([O-:17])=[O:15])[C:5]([F:8])=[CH:4][C:3]=1[CH3:9]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred solution of 1-bromo-4-fluoro-2-methyl-benzene (15.0 g, 79.8 mmol) in dichloromethane (300 mL) was added nitronium tetrafluoroborate (11.7 g, 87.8 mmol) in portions at 0° C. The mixture was heated at reflux for 5 h and was then poured into ice water. The organic layer was separated and the aqueous phase was extracted with dichloromethane (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated under reduced pressure to give crude 1-bromo-4-fluoro-2-methyl-5-nitrobenzene (18.0 g), which was used directly in the next step.
Aufarbeitung
- temperatureThe mixture was heated
- temperatureat reflux for 5 h
- customThe organic layer was separated
- extractionthe aqueous phase was extracted with dichloromethane (100 mL×3)
- dry with materialThe combined organic layers were dried over anhydrous Na2SO4
- customevaporated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-ebdb4a4f930d45d5ad488e675eeaa94a
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08846753B2
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