Reacción #9982

ord-82f6431d8ef44e6fb7bc43c55597e2a3

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónAt the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure
  2. 2
    workup.DISSOLUTIONthe resulting residue was dissolved in dichloromethane (2 ml)
  3. 3
    workup.STIRRINGthe resulting mixture was stirred at room temperature for 2 hours
  4. 4
    Extracciónextracted with dichloromethane
  5. 5
    LavadoThe organic layer was washed with water
  6. 6
    Secadodried over anhydrous magnesium sulfate
  7. 7
    Otrothe solvent was removed by distillation under reduced pressure

Procedimiento

(±)-1-(t-Butoxycarbonyl)-2-(2-oxo-3-butenyl)pyrrolidine (206 mg (10.86 mmol), prepared as described in Reference example 1–2)) was dissolved in tetrahydrofuran (2 ml). To the solution was added 4-methylthiophenol (107 mg, 0.86 mmol), and the resulting mixture was stirred at room temperature for 2 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure, and the resulting residue was dissolved in dichloromethane (2 ml). To the resulting mixture was added 70 wt % m-chloroperbenzoic acid (468 mg, 1.894 mmol) by portions under ice cooling, and the resulting mixture was stirred at room temperature for 2 hours. To the mixture were added an aqueous solution of 10% sodium thiosulfate and a saturated aqueous solution of sodium hydrogencarbonate in that order, and the resulting mixture was stirred and extracted with dichloromethane. The organic layer was washed with water, dried over anhydrous magnesium sulfate and the solvent was removed by distillation under reduced pressure, to give the title compound (322 mg) as a colorless oil (yield 94%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091352B2uspto-grants-2006_08