Reacción #54851

ord-24c0bba72cee4fa2b7f843525056e36e

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroIn a suitable container (erlenmeyer flasks are suitable
  2. 2
    Temperaturaany other vessel which may be heated could
  3. 3
    Temperaturaheat on a steam bath
  4. 4
    workup.ADDITIONAt the end of the heating period add 650 ml
  5. 5
    workup.DISTILLATIONof distilled
  6. 6
    workup.ADDITIONdeionized water and then add 6 N NaOH slowly with extremely rapid stirring
  7. 7
    workup.ADDITIONthe addition when the pH
  8. 8
    Otrocollect the supernate
  9. 9
    Filtraciónby filtration
  10. 10
    workup.WAITto stand for a day
  11. 11
    Filtraciónfilter with 2 g of activated carbon by gravity through a tight filter paper
  12. 12
    Otroto produce a decolorized filtrate
  13. 13
    ConcentraciónAfter determination of the 1,2,4,6-tetraphenylpyridinium acetate concentration (vide infra)
  14. 14
    workup.ADDITIONdilute the solution to the desired
  15. 15
    Concentraciónconcentration
  16. 16
    workup.DISTILLATIONwith distilled

Procedimiento

In a suitable container (erlenmeyer flasks are suitable but any other vessel which may be heated could serve as well) place 33.33 g of recrystallized 1,3,5-triphenyl-2-penten-1,5-dione and 9.31 g of purified aniline. To this mixture add 37.5 ml of glacial acetic acid and heat on a steam bath or other suitable heating source for two hours. At the end of the heating period add 650 ml of distilled, deionized water and then add 6 N NaOH slowly with extremely rapid stirring. Discontinue the addition when the pH, indicated by a glass electrode, reaches 7.0. Allow any precipitate to settle, collect the supernate by filtration and retain this filtrate. Allow the filtrate to stand for a day, and then filter with 2 g of activated carbon by gravity through a tight filter paper to produce a decolorized filtrate. After determination of the 1,2,4,6-tetraphenylpyridinium acetate concentration (vide infra) dilute the solution to the desired concentration with distilled, deionized water. The 1,2,4,6-tetraphenylpyridinium cation is characterized through its perchlorate and perrhenate salts by elemental analysis.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04150233uspto-grants-1979_04