Reacción #216539

ord-6261e6ad67cc4ea18f5f2c8f819a22af

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture was heated under argon for 24 hrs
  2. 2
    TemperaturaThe reaction mixture was cooled
  3. 3
    Lavadowashed with saturated aqueous sodium bicarbonate
  4. 4
    SecadoThe organic layer was dried over magnesium sulfate
  5. 5
    Filtraciónfiltered
  6. 6
    Otroevaporated to dryness under vacuum
  7. 7
    Otroto give an off-white solid
  8. 8
    OtroThe crude product was recrystallized from methanol

Procedimiento

Dodecanoyl chloride (2.95 ml, 12.8 mmol) was added to a suspension of 2,4,6-triiodophenol (6.0 g, 12.7 mmol) in refluxing acetonitrile (50 ml) and the mixture was heated under argon for 24 hrs. The reaction mixture was cooled and washed with saturated aqueous sodium bicarbonate. The organic layer was dried over magnesium sulfate, filtered, and evaporated to dryness under vacuum to give an off-white solid. The crude product was recrystallized from methanol to give 6.9 g (83%) of the desired ester, mp 68°-69° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05468466uspto-grants-1995_11