Reacción #1674347

ord-3b523f77d274452a835a8771de0decc0

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadowashed with brine until the aqueous washes
  2. 2
    SecadoThe diethyl ether layer is dried (magnesium sulfate)
  3. 3
    Filtraciónfiltered
  4. 4
    Concentraciónconcentrated

Procedimiento

Jones reagent (chromium trioxide-sulfuric acid-water), 4.4 mL (8.85 mmol), is added dropwise to a 0° C. solution of (±)-cis-4-(2-oxoethyl)-1,5-dioxaspiro[5.5]undecane-2-acetonitrile, 3.62 g (12.6 mmol), dissolved in 30 mL of acetone until the orange color is not discharged. After stirring a further 15 minutes, the mixture is poured into 300 mL of diethyl ether and washed with brine until the aqueous washes are colorless. The diethyl ether layer is dried (magnesium sulfate), filtered, and concentrated to provide 3.65 g of (±)-cis-4-(cyanomethyl)-1,5dioxaspiro[5.5]undecane-2-acetic acid as a yellow solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05216174uspto-grants-1993_06