Reacción #68008

ord-0c9d7f38499840a9bd74ad95e8a955b4

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added
  2. 2
    OtroThe organic layer was separated
  3. 3
    Extracciónthe aqueous layer was extracted with chloroform
  4. 4
    Lavadothe resultant solution was washed with an aqueous saturated sodium chloride solution
  5. 5
    Secadodried over anhydrous magnesium sulfate
  6. 6
    Otrothe solvent was removed under reduced pressure

Procedimiento

To 14 mL of a chloroform solution containing 0.90 g of 4-chloro-7-trifluoromethylquinoline, 1.04 g of m-chloroperbenzoic acid was added, and the mixture was stirred at room temperature for 3.5 hours. The reaction mixture was added with 15 mL of an aqueous saturated sodium hydrogen carbonate solution. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain a yellow solid, 4-chloro-7-trifluoromethylquinoline N-oxide.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524738B2uspto-grants-2013_09