Reacción #216539
ord-6261e6ad67cc4ea18f5f2c8f819a22af
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturathe mixture was heated under argon for 24 hrs
- 2TemperaturaThe reaction mixture was cooled
- 3Lavadowashed with saturated aqueous sodium bicarbonate
- 4SecadoThe organic layer was dried over magnesium sulfate
- 5Filtraciónfiltered
- 6Otroevaporated to dryness under vacuum
- 7Otroto give an off-white solid
- 8OtroThe 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.