Reacción #5674

ord-1c87a99897674504b9f67b900895e476

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónfiltered
  2. 2
    Lavadowashed with acetone
  3. 3
    Otroevaporated to a brown oil
  4. 4
    OtroThe oil is purified by flash chromatography
  5. 5
    Lavadoeluting with 5 percent acetone in toluene
  6. 6
    Otroevaporated

Procedimiento

A mixture of 240 mg of the above oxazolidinone, 234 mg of diethyl bromomalonate, 450 mg of anhydrous potassium carbonate and 10 ml of acetone is stirred overnight, filtered, washed with acetone and evaporated to a brown oil. The oil is purified by flash chromatography, eluting with 5 percent acetone in toluene. The pure fractions are combined and evaporated giving 237 mg of (R,R)-5-(3-chlorophenyl)-2-oxo-3-oxazolidinyl)propyl)-1,3-benzodioxole-2,2-dicarboxylic acid, diethyl ester as a colorless oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05245053uspto-grants-1993_09