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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 719048생성일: 2026년 10월 26일

Potassium Carbonate → 12,12-Dimethyl-10-phenyl-7-(4-diphenylamino-phenyl)-10,12-dihydroindeno[2,1-b]carbazole

https://huagongshe.com/reaction/719048

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-(Diphenylamino)phenylboronic Acid (contains varying amounts of Anhydride)HCID 12166934—
반응물Toluene ethanolHCID 21863594—
반응물7-Bromo-12,12-dimethyl-10-phenyl-10,12-dihydroindeno[2,1-b]carbazoleHCID 86685015—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물12,12-Dimethyl-10-phenyl-7-(4-diphenylamino-phenyl)-10,12-dihydroindeno[2,1-b]carbazoleHCID 8957261858.4%

반응 조건

온도73 °C

반응 단계

7-Bromo-12,12-dimethyl-10-phenyl-10,12-dihydroindeno[2,1-b]carbazole synthesized in Example 1 (2.0 g), 4-diphenylamino-phenylboronic acid (1.32 g), a toluene/ethanol (4/1, v/v) mixed solvent (15 ml), and a 2M potassium carbonate aqueous solution (3.4 ml) were added to a nitrogen-substituted reaction vessel and aerated with nitrogen gas for 30 min under ultrasonic irradiation. The mixture was heated after adding tetrakis(triphenylphosphine)palladium (0.26 g), and stirred at 73° C. for 5 hours. After the mixture was cooled to a room temperature, toluene (30 ml) and water (20 ml) were added to perform liquid separation in order to collect an organic layer. The organic layer was washed with saturated brine, dehydrated with anhydrous magnesium sulfate, and concentrated under reduced pressure to obtain a crude product. The crude product was purified by column chromatography (carrier: silica gel; eluent: toluene/n-hexane) to obtain a pale yellowish white powder of 12,12-dimethyl-10-phenyl-7-(4-diphenylamino-phenyl)-10,12-dihydroindeno[2,1-b]carbazole (1.6 g; yield 58.4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09196837B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-9ce390a62436465cb048a628dc408cbe
출처 메모uspto-grants-2015_11