Réaction #50957

ord-8fd396eb07384b19b02d269c9665c82c

Conditions de réaction

Température
-78°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe reaction is quenched by slow addition of a saturated aqueous solution of ammonium chloride (20 mL) The cooling bath
  2. 2
    Autreis removed
  3. 3
    Températureto warm to ambient temperature with vigorous stirring
  4. 4
    AutreThe solvent is removed in vacuo
  5. 5
    workup.ADDITIONthe residue diluted with dichloromethane (200 mL)
  6. 6
    LavageThe mixture is washed with water (150 mL) and saturated aqueous sodium bicarbonate solution (150 mL), water and brine
  7. 7
    ExtractionThe combined aqueous layers are extracted with dichloromethane (200 mL), water (150 mL), NaCl (sat.) (200 mL)
  8. 8
    Séchagedried over sodium sulfate
  9. 9
    Filtrationfiltered
  10. 10
    Concentrationconcentrated in vacuo

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06849627B2uspto-grants-2005_02