Reacción #1543037
ord-4719ee4de4624803a19d4699cd571b1f
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1OtroA 200-milliliter 3-necked round bottom flask equipped with a mechanical stirrer
- 2Temperaturareflux condenser, and argon inlet
- 3Otrowas purged with argon
- 4TemperaturaThe mixture was cooled to about 100° C.
- 5OtroThe resulting two phase mixture was transferred into a separatory funnel
- 6Otrothe layers separated
- 7Lavadowas washed with water
- 8workup.ADDITIONtreated with 25 grams of alumina under an argon atmosphere
- 9Filtraciónfiltered
- 10OtroThe filtrate was then evaporated
- 11Otrothe residue was recrystallized from cyclohexane
Procedimiento
A 200-milliliter 3-necked round bottom flask equipped with a mechanical stirrer, reflux condenser, and argon inlet was purged with argon and then charged with 5,11-dihydroindolo[3,2-b]carbazole (5.1 grams, 0.02 mol), 3-iodotoluene (8.69 grams, 0.04 mol), copper sulfate pentahydrate (0.25 gram, 1.0 mmol), potassium carbonate (5.52 grams, 0.04 mol), and n-tridecane (5.0 milliliters). Under an argon atmosphere, the reaction mixture was heated to about 250° C. with a heating mantle and allowed to proceed at this temperature to completion in about 6 hours. The mixture was cooled to about 100° C., and 100 milliliters of toluene and 15 milliliters of water were then added with vigorous stirring. The resulting two phase mixture was transferred into a separatory funnel and the layers separated. The organic phase, which contained the desired product, was washed with water, and treated with 25 grams of alumina under an argon atmosphere, and filtered. The filtrate was then evaporated and the residue was recrystallized from cyclohexane to provide 6.8 grams of pure, about 99.9 percent, 5,11-di-m-tolyl-5,11-dihydroindolo-[3,2-b]carbazole (1).