Reacción #5800

ord-bb6410a0138c4ef592942e2835802a42

Ecuación de reacción

CC(C)=O.O=S(=O)(O)O.[O]=[Cr](=[O])=[O]
Jones reagent
N#CC[C@H]1C[C@@H](CC=O)OCO1
(±)-cis-6-(2-oxoethyl)-1,3-dioxane-4-acetonitrile
CCOCC
diethyl ether
N#CC[C@@H]1C[C@H](CC(=O)O)OCO1
(±)-cis-6-(cyanomethyl)-1,3-dioxane-4-acetic acid

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), 3.8 mL (97.6 mmol), is added dropwise to a 0° C. solution of (±)-cis-6-(2-oxoethyl)-1,3-dioxane-4-acetonitrile, 1.29 g of (7.6 mmol), dissolved in 50 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 1.2 g of (±)-cis-6-(cyanomethyl)-1,3-dioxane-4-acetic acid as a colorless solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05245047uspto-grants-1993_09