Reacción #56361

ord-2366a6ae4634412587007d52d3c06a6a

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaby heating
  2. 2
    workup.ADDITIONa mixture of 8.0 g
  3. 3
    OtroThe liberated monomer was bubbled (argon stream) into 4.8 g
  4. 4
    Otroat 120°
  5. 5
    Temperaturathe solution was heated at 120° for an additional 45 minutes
  6. 6
    workup.DISTILLATIONDistillation
  7. 7
    Otroafforded 1.32 g

Procedimiento

Monomeric glyoxal was generated by heating a mixture of 8.0 g. of glyoxal hydrate (0.117 mol. of monomer) and 48.0 g. of phosphorus pentoxide over a gentle flame over 35 minutes. The liberated monomer was bubbled (argon stream) into 4.8 g. (0.04 mol) of 1-ethoxy-1,3-pentadiene (purity 92.3%) at 120°. After all the monomer had been generated, the solution was heated at 120° for an additional 45 minutes. Distillation afforded 1.32 g. of the pyran (b0.07 =56°, purity 91%) and 1.86 g. of recovered diene (yield based on diene-32%, based on glyoxal=6.6%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04225514uspto-grants-1980_09