Reaktion #341385

ord-f5449b15f7f64e24b9378363a2e8677e

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07875606B2uspto-grants-2011_01