Reaktion #2487392
ord-df8e613e5a0e4961a1f33ca455f88d54
Reaktionsgleichung
4-bromo-2,2′-bipyridyl-N-oxide
PCl3
→
4-bromo-2,2′-bipyridyl
Ausbeute 85.0%
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeat room temperature
- 2TemperaturThe mixture was refluxed for 2 h under N2
- 3SonstigeThe aqueous layer was separated
- 4ExtraktionThe CHCl3, layer was extracted three times with H2O (3×60 mL)
- 5FiltrationThe resulting white precipitate was collected by suction filtration
- 6Waschenwashed with H2O (30 mL)
- 7Sonstigedried under vacuum at 50° C. for 24 h
Vorschrift
To a stirred suspension of 4-bromo-2,2′-bipyridyl-N-oxide in 60 mL CHCl3, was added 12 mL PCl3, at room temperature. The mixture was refluxed for 2 h under N2 and then cooled to room temperature. The reaction mixture was poured into 100 mL ice/water. The aqueous layer was separated and saved. The CHCl3, layer was extracted three times with H2O (3×60 mL) and then discarded. The combined aqueous solution was neutralized with NaHCO3 powder to about pH 7-8. The resulting white precipitate was collected by suction filtration, washed with H2O (30 mL) and then dried under vacuum at 50° C. for 24 h. Yield: 85%.