Reacción #341385

ord-f5449b15f7f64e24b9378363a2e8677e

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe mixture was stirred at room temperature for 2 hours
  2. 2
    Otroto give rise
  3. 3
    Otroto a reaction
  4. 4
    OtroAfter the completion of the reaction
  5. 5
    LavadoThe resulting organic layer was washed with an aqueous sodium chloride solution
  6. 6
    Secadoby drying over anhydrous magnesium sulfate
  7. 7
    workup.DISTILLATIONThe resulting solution was subjected to reduced pressure distillation
  8. 8
    Otroto remove the solvent
  9. 9
    OtroThe residue was purified by silica gel column chromatography

Procedimiento

1.2 g (15.0 mmoles) of sodium hydrosulfide hydrate (purity: 70%) was added into a solution of 2.1 g (10.0 mmoles) of 5-chloromethyl-5-methyl-3-methylsulfonyl-2-isoxazoline dissolved in 20 ml of N,N-dimethylformamide. The mixture was stirred for 2 hours. Then, there were added 2.1 g (15.0 mmoles) of anhydrous potassium carbonate, 2.3 g (15.0 mmoles) of Rongalit and 2.8 g (10.0 mmoles) of 4-bromomethyl-5-chloro-1-methyl-3-trifluoromethyl-1H-pyrazole. The mixture was stirred at room temperature for 2 hours to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water and extraction with ethyl acetate was conducted. The resulting organic layer was washed with an aqueous sodium chloride solution, followed by drying over anhydrous magnesium sulfate. The resulting solution was subjected to reduced pressure distillation to remove the solvent contained therein. The residue was purified by silica gel column chromatography to obtain 3.3 g (yield: 100.0%) of 3-(5-chloro-1-methyl-3-trifluoromethyl-1H-pyrazol-4-ylmethylthio)-5-chloromethyl-5-methyl-2-isoxazoline.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07875606B2uspto-grants-2011_01