Reaktion #1543038

ord-f2ab0cf4857b40688e5c7d4c2ee3e7e7

Lösungsmittel

Reaktionsbedingungen

Temperatur
250°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA 200 milliliter 3-necked round bottom flask equipped with a mechanical stirrer
  2. 2
    Temperaturreflux condenser, and argon inlet
  3. 3
    Sonstigewas purged with argon
  4. 4
    TemperaturThe reaction mixture was cooled to about 100° C.
  5. 5
    SonstigeThe resulting two phase mixture was transferred into a separatory funnel
  6. 6
    Sonstigethe layers separated
  7. 7
    Waschenwas washed with water
  8. 8
    workup.ADDITIONtreated with 25 grams of alumina under an argon atmosphere
  9. 9
    Filtrationfiltered
  10. 10
    SonstigeThe filtrate was then evaporated
  11. 11
    Sonstigethe residue was recrystallized from toluene

Vorschrift

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), 1-iodonaphthalene (10.16 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 reaction mixture was cooled to about 100° C., and 100 milliliters of toluene and 15 milliliters of water were then added with vigorous stirring for 30 minutes. The resulting two phase mixture was transferred into a separatory funnel and the layers separated. The organic phase which contains the desired product was washed with water, treated with 25 grams of alumina under an argon atmosphere, and filtered. The filtrate was then evaporated and the residue was recrystallized from toluene to provide 2.5 grams of pure, about 99.9 percent, 5,11-di-1-naphthyl-5,11-dihydroindolo[3,2-b]carbazole (3).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05843607uspto-grants-1998_12