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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1455856생성일: 2026년 10월 27일

1-Iodonaphthalene → 5,11-Di-1-naphthyl-5,11-dihydroindolo[3,2-b]carbazole

https://huagongshe.com/reaction/1455856

반응식

참여 물질

역할이름HCID투입량
반응물1-IodonaphthaleneHCID 7004—
반응물Potassium CarbonateHCID 11430—
반응물TridecaneHCID 12388—
반응물5,11-Dihydroindolo[3,2-b]carbazoleHCID 95838—
촉매Copper sulfate pentahydrateHCID 24463—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물5,11-Di-1-naphthyl-5,11-dihydroindolo[3,2-b]carbazoleHCID 22598595—

반응 조건

온도250 °C

반응 단계

A 200 milliliter 3-necked round bottom flask equipped with a mechanical stirrer, reflux condenser, and argon inlet was purged with argon and then charged with 5,11-dihydroindolo[3,2-b]carbazole (5.1 grams, 0.02 mol), 1-iodonaphthalene (10.16 grams, 0.04 mol), copper sulfate pentahydrate (0.25 gram, 1.0 mmol), potassium carbonate (5.52 grams, 0.04 mol), and n-tridecane (5.0 milliliters). Under an argon atmosphere, the reaction mixture was heated to about 250° C. with a heating mantle and allowed to proceed at this temperature to completion in about 6 hours. The reaction mixture was cooled to about 100° C., and 100 milliliters of toluene and 15 milliliters of water were then added with vigorous stirring for 30 minutes. The resulting two phase mixture was transferred into a separatory funnel and the layers separated. The organic phase which contains the desired product was washed with water, treated with 25 grams of alumina under an argon atmosphere, and filtered. The filtrate was then evaporated and the residue was recrystallized from toluene to provide 2.5 grams of pure, about 99.9 percent, 5,11-di-1-naphthyl-5,11-dihydroindolo[3,2-b]carbazole (3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05843607
출처 데이터셋uspto-grants-1998_12
ORD IDord-f2ab0cf4857b40688e5c7d4c2ee3e7e7
출처 메모uspto-grants-1998_12