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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64546생성일: 2026년 10월 24일

Potassium Carbonate → 4-(9H-Carbazol-3-yl)dibenzofuran

https://huagongshe.com/ko/reaction/64546

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Tri-o-tolylphosphineHCID 80271—
반응물3-BromocarbazoleHCID 252446—
반응물Dibenzofuran-4-boronic acidHCID 2734328—
촉매palladium(II) acetateHCID 167845—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물4-(9H-Carbazol-3-yl)dibenzofuranHCID 6669187785%

반응 조건

온도80 °C

반응 단계

In a 200-mL three-neck flask were put 2.0 g (8.1 mmol) of 3-bromocarbazole, 1.7 g (8.1 mmol) of dibenzofuran-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 20 mL of toluene, 20 mL of ethanol, and 15 mL (0.2 mol) of an aqueous potassium carbonate solution (2.0 mol/L). In the flask, the mixture was degassed by being stirred under reduced pressure. Then, 23 mg (0.10 mmol) of palladium(II) acetate was added to this mixture, and then the mixture was refluxed at 80° C. After the reflux, the mixture was cooled to room temperature, and then the obtained 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 2.3 g of a white solid was obtained in 85% yield. The synthesis scheme of Step 1 is illustrated in (a-2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09450188B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-86f3b9dd3e77472b8118478b6c030341
출처 메모uspto-grants-2016_09