Reacción #4685

ord-e9adca82e09c421dacd1f2f89a865ee9

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónconcentrated by evaporation in a high vacuum
  2. 2
    workup.DISSOLUTIONThe residue is dissolved in ethyl acetate
  3. 3
    Lavadowashed with 0.1N hydrochloric acid and water
  4. 4
    Secadodried over sodium sulphate
  5. 5
    Concentraciónconcentrated by evaporation
  6. 6
    Otropurified by chromatography on silica gel with toluene

Procedimiento

2(R,S)-Cyanomethyl-3-α-naphthylpropionic acid: 3.0 g of α-naphthylmethylmalonic acid diethyl ester and, after 30 minutes, 0.6 ml of chloroacetonitrile are added to a stirred suspension of 0.44 g of sodium hydride dispersion in 50 ml of DMF. The reaction mixture is stirred for 1 hour at 50° and then concentrated by evaporation in a high vacuum. The residue is dissolved in ethyl acetate, washed with 0.1N hydrochloric acid and water, dried over sodium sulphate, concentrated by evaporation and purified by chromatography on silica gel with toluene, yielding cyanomethyl-(α-naphthylmethyl)-malonic acid diethyl ester.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04727060uspto-grants-1988_02