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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1455856Erstellt: 26. Oktober 2026

1-Iodonaphthalene → 5,11-Di-1-naphthyl-5,11-dihydroindolo[3,2-b]carbazole

https://huagongshe.com/reaction/1455856

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-IodonaphthaleneHCID 7004—
EduktPotassium CarbonateHCID 11430—
EduktTridecaneHCID 12388—
Edukt5,11-Dihydroindolo[3,2-b]carbazoleHCID 95838—
KatalysatorCopper sulfate pentahydrateHCID 24463—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt5,11-Di-1-naphthyl-5,11-dihydroindolo[3,2-b]carbazoleHCID 22598595—

Reaktionsbedingungen

Temperatur250 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05843607
Quelldatensatzuspto-grants-1998_12
ORD IDord-f2ab0cf4857b40688e5c7d4c2ee3e7e7
Quellennotizuspto-grants-1998_12