Reacción #7750

ord-dda017fe43b8478fafb3335b9df58960

Disolventes

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe reaction is quenched by slow addition of a saturated aqueous solution of ammonium chloride (20 mL)
  2. 2
    OtroThe cooling bath is removed
  3. 3
    Temperaturato warm to ambient temperature with vigorous stirring
  4. 4
    OtroThe solvent is removed in vacuo
  5. 5
    workup.ADDITIONthe residue diluted with dichloromethane (200 mL)
  6. 6
    LavadoThe mixture is washed with water (150 mL) and saturated aqueous sodium bicarbonate solution (150 mL), water and brine
  7. 7
    ExtracciónThe combined aqueous layers are extracted with dichloromethane (200 mL), water (150 mL), NaCl (sat.) (200 mL)
  8. 8
    Secadodried over sodium sulfate
  9. 9
    Filtraciónfiltered
  10. 10
    Concentraciónconcentrated in vacuo

Procedimiento

4-Oxo-pyrazolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester, 27, (5.0 g, 15.6 mmol) is dissolved in tetrahydrofuran (150 mL) and the solution cooled to −78° C. A 5.0 M solution of borane-dimethyl sulfide complex in ether (6.24 mL, 31.2 mmol) is added dropwise via syringe. After 40 minutes at −78° C., the reaction is quenched by slow addition of a saturated aqueous solution of ammonium chloride (20 mL). The cooling bath is removed, and the mixture allowed to warm to ambient temperature with vigorous stirring. The solvent is removed in vacuo and the residue diluted with dichloromethane (200 mL). The mixture is washed with water (150 mL) and saturated aqueous sodium bicarbonate solution (150 mL), water and brine. The combined aqueous layers are extracted with dichloromethane (200 mL), water (150 mL), NaCl (sat.) (200 mL), dried over sodium sulfate, filtered and concentrated in vacuo to afford 4.66 g (93% yield) of the desired product as a clear, viscous oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07087615B2uspto-grants-2006_08