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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64545생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Tri-o-tolylphosphineHCID 80271—
반응물3-BromocarbazoleHCID 252446—
반응물Dibenzothiophene-4-boronic acidHCID 2734329—
촉매palladium(II) acetateHCID 167845—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물3-(Dibenzothiophen-4-yl)-9H-carbazoleHCID 6669187232%

반응 조건

온도110 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09450188B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-ee7dbb42a65e420c928d59e5652a9c9b
출처 메모uspto-grants-2016_09