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HRID 64545作成日:2026年10月24日

Potassium Carbonate → 3-(Dibenzothiophen-4-yl)-9H-carbazole

https://huagongshe.com/ja/reaction/64545

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Tri-o-tolylphosphineHCID 80271—
反応物3-BromocarbazoleHCID 252446—
反応物Dibenzothiophene-4-boronic acidHCID 2734329—
触媒palladium(II) acetateHCID 167845—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
生成物3-(Dibenzothiophen-4-yl)-9H-carbazoleHCID 6669187232%

反応条件

温度110 °C

反応手順

In a 200-mL three-neck flask were put 3.0 g (12 mmol) of 3-bromocarbazole, 2.8 g (12 mmol) of dibenzothiophene-4-boronic acid, and 150 mg (0.5 mol) of tri(ortho-tolyl)phosphine, and the air in the flask was replaced with nitrogen. To this mixture were added 40 mL of toluene, 40 mL of ethanol, and 15 mL (2.0 mol/L) of an aqueous potassium carbonate solution. In the flask, the mixture was degassed by being stirred under reduced pressure. After the degassing, replacement with nitrogen was performed, and 23 mg (0.10 mmol) of palladium(II) acetate was added to this mixture, and then the mixture was refluxed at 110° C. for 3 hours. After the reflux, the mixture was cooled to room temperature, and then the precipitated solid was collected by suction filtration. The collected solid was dissolved in 100 mL of toluene, and this solution was filtered through Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135), and alumina. The solid obtained by concentration of the obtained filtrate was recrystallized from toluene/hexane, so that 1.4 g of a white solid, which was the object of the synthesis, was obtained in 32% yield. The synthesis scheme of Step 1 is illustrated in (a-1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09450188B2
出典データセットuspto-grants-2016_09
ORD IDord-ee7dbb42a65e420c928d59e5652a9c9b
出典メモuspto-grants-2016_09