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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 558042생성일: 2026년 10월 26일

Tris(1,1-dimethylethyl)phosphine → 11-(4-Carbazolylphenyl)indolo[2,3-a]carbazole

https://huagongshe.com/reaction/558042

반응식

참여 물질

역할이름HCID투입량
반응물Tris(1,1-dimethylethyl)phosphineHCID 83681—
반응물Indolo[2,3-a]carbazoleHCID 21882147—
반응물4-CarbazolylbromobenzeneHCID 23143955—
반응물Sodium t-butoxideHCID 23676156—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매O-XyleneHCID 7237—
생성물11-(4-Carbazolylphenyl)indolo[2,3-a]carbazoleHCID 6693759847%

반응 조건

온도60 °C

반응 단계

In a 100-ml three-necked flask were placed 0.21 g (0.94 mmole) of palladium(II) acetate, 20 ml of xylene, and 0.76 g (3.76 mmoles) of tri-tert-butylphosphine and the mixture was heated at 60° C. with stirring for 30 minutes. The resulting solution was sent into a solution that had been prepared by dissolving 4.61 g (0.0180 mole) of indolo[2,3-a]carbazole, 5.8 g (0.018 mole) of 4-carbazolylbromobenzene, and 7.7 g (0.080 mole) of sodium tert-butoxide in 180 ml of xylene and heated at 60° C. in a stream of nitrogen and the combined solution was heated up to 130° C. and kept at this temperature for 5 hours with stirring. The solution was cooled to room temperature, 200 ml of water was added, and the organic layer was separated and concentrated under reduced pressure to give a crude product. The crude product was purified by crystallization from dichloromethane and ethanol, the solvent was distilled off under reduced pressure, and 4.2 g (0.0084 mole, 47% yield) of 11-(4-carbazolylphenyl)indolo[2,3-a]carbazole was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08062769B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-6858f3c062f24685a3d9f60c0b864aed
출처 메모uspto-grants-2011_11