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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455855Generated: October 25, 2026

Potassium Carbonate → 5,11-Di-m-tolyl-5,11-dihydroindolo[3,2-b]carbazole

https://huagongshe.com/reaction/1455855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-IodotolueneHCID 12268—
ReactantTridecaneHCID 12388—
Reactant5,11-Dihydroindolo[3,2-b]carbazoleHCID 95838—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5,11-Di-m-tolyl-5,11-dihydroindolo[3,2-b]carbazoleHCID 15404959—

Reaction Conditions

Temperature250 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843607
Source datasetuspto-grants-1998_12
ORD IDord-4719ee4de4624803a19d4699cd571b1f
Source noteuspto-grants-1998_12