Reacción #75250

ord-d83bb453aaa44b2cb4964bca2e51c0d9

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otro/in2 and 25° C
  2. 2
    Otrothe catalyst is removed by filtration
  3. 3
    Otrothe solvent is evaporated under vacuum

Procedimiento

1-(2-Tetrahydropyranyloxy)-4-acetoxy-5-propoxy-2-pentyne (10.8 g., 0.04 mole) is dissolved in ethyl acetate (100 ml.). 5% Palladium on carbon is added and the mixture is hydrogenated on the Parr apparatus at an initial pressure of 41 lbs./in2 and 25° C. When 0.08 mole of hydrogen is absorbed, the catalyst is removed by filtration and the solvent is evaporated under vacuum to give the title compound as a light orange residual oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04175203uspto-grants-1979_11