Reacción #63724

ord-39749d82d8984a9b830f19e45fb8b4be

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture is heated
  2. 2
    Temperaturaunder reflux for 2 hours
  3. 3
    Concentraciónconcentrated in a rotary evaporator
  4. 4
    OtroThe residue is chromatographed on silica gel with ethyl acetate/methylene chloride (3:1) as the elution agent
  5. 5
    Otrothe pressure being produced with nitrogen gas
  6. 6
    OtroBy recrystallization from ether

Procedimiento

A solution of 24 g (0.22 mol) of 2,3-dimethylpyridine in 100 ml of methylene chloride is treated while cooling with ice with a solution of 46.6 g (0.27 mol) of m-chloroperbenzoic acid in 100 ml of methylene chloride. The reaction mixture is heated under reflux for 2 hours and concentrated in a rotary evaporator. The residue is chromatographed on silica gel with ethyl acetate/methylene chloride (3:1) as the elution agent, the medium pressure flash chromatography method being used and the pressure being produced with nitrogen gas. By recrystallization from ether there is obtained 2,3-dimethylpyridine 1-oxide of melting point 56°.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04766133uspto-grants-1988_08