Reacción #168876

ord-dbb251982fd84cea88e23d9109cbe504

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaunder cooling on ice
  2. 2
    ExtracciónThe water layer was extracted with chloroform two times
  3. 3
    SecadoThe organic layer was dried over anhydrous sodium sulfate
  4. 4
    workup.DISTILLATIONthe solvent was then distilled away

Procedimiento

The above 3-chloro-4-methoxy-2,5-dimethylpyridine (181 mg) was dissolved in 5 ml of dichloromethane, and urea peroxide (169 mg) and phthalic anhydride (219 mg) were then added to the solution. The resulting mixture was stirred at room temperature for 2.5 hours. Thereafter, a saturated aqueous sodium thiosulfate solution was added to the reaction solution under cooling on ice, and the resulting mixture was then diluted with chloroform. The water layer was extracted with chloroform two times. The organic layer was dried over anhydrous sodium sulfate, and the solvent was then distilled away, so as to obtain the title compound (181 mg) as a solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08846703B2uspto-grants-2014_09