Reacción #87874

ord-9ba0b5fb06a2412a81fa7bb65b7f0d92

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe vial was closed
  2. 2
    Otropurged with nitrogen for 10 min
  3. 3
    workup.ADDITIONafter which the vial was charged with DMF (4.5 mL) and water (0.5 mL)
  4. 4
    workup.STIRRINGto stir under nitrogen for 35 min until a very dark blue/black solution
  5. 5
    workup.STIRRINGto stir at 27° C. for 5.5 h
  6. 6
    OtroThe crude reaction mixture
  7. 7
    Filtraciónwas filtered through a medium frit
  8. 8
    Filtraciónfilter
  9. 9
    Lavadothe filter cake was washed with DMF (2×)
  10. 10
    workup.ADDITIONThe resulting filtrate was diluted with an equal volume of 10% HCl (aq)
  11. 11
    Otroto yield a clear, light yellow solution which
  12. 12
    workup.STIRRINGto stir overnight at ambient temperature
  13. 13
    FiltraciónThe white solid was collected by vacuum filtration
  14. 14
    Otrowas dried in an inert heating oven (50° C.; 1 h)

Procedimiento

An 8 mL scintillation vial was charged with NiCl2.6H2O (87.8 mg, 0.369 mmol) and 2,2′-bipyridine (119.2 mg, 0.763 mmol). The vial was closed and purged with nitrogen for 10 min, after which the vial was charged with DMF (4.5 mL) and water (0.5 mL). The mixture was allowed to stir for 5 min until a clear, bright blue solution was present. To the vial was added zinc dust (1.657 g, 25.3 mmol), and the mixture was allowed to stir under nitrogen for 35 min until a very dark blue/black solution was present. Solid 3,4,5,6-tetrachloropicolinic acid (0.831 g, 3.2 mmol) was added through the top of the reactor. The reaction mixture was allowed to stir at 27° C. for 5.5 h. The crude reaction mixture was filtered through a medium frit filter, and the filter cake was washed with DMF (2×). The resulting filtrate was diluted with an equal volume of 10% HCl (aq) to yield a clear, light yellow solution which was allowed to stir overnight at ambient temperature. The white solid was collected by vacuum filtration and was dried in an inert heating oven (50° C.; 1 h) to give the title compound (0.60 g, 83.1%) that was 69% pure as analyzed by calibrated HPLC.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09440923B2uspto-grants-2016_09