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HRID 1455855作成日:2026年10月27日

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

https://huagongshe.com/reaction/1455855

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物3-IodotolueneHCID 12268—
反応物TridecaneHCID 12388—
反応物5,11-Dihydroindolo[3,2-b]carbazoleHCID 95838—
触媒Copper sulfate pentahydrateHCID 24463—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物5,11-Di-m-tolyl-5,11-dihydroindolo[3,2-b]carbazoleHCID 15404959—

反応条件

温度250 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05843607
出典データセットuspto-grants-1998_12
ORD IDord-4719ee4de4624803a19d4699cd571b1f
出典メモuspto-grants-1998_12