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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1585961생성일: 2026년 10월 27일

Potassium Carbonate → 5,11-Di-m-tolyl-5,11-dihydroindolo[3,2-b]carbazole

https://huagongshe.com/reaction/1585961

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-IodotolueneHCID 12268—
반응물TridecaneHCID 12388—
반응물5,11-Dihydroindolo[3,2-b]carbazoleHCID 95838—
촉매Copper sulfate pentahydrateHCID 24463—
생성물5,11-Di-m-tolyl-5,11-dihydroindolo[3,2-b]carbazoleHCID 15404959—

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), 3-iodotoluene (8.69 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 that temperature until chromatographic analysis indicated that the reaction was complete after approximately 6 hours. The heating mantle was removed and the mixture was cooled to about 100° C., and 100 milliliters of toluene and 15 milliliters of water were then added with vigorous stirring. The resulting two phase mixture was transferred into a separatory funnel and the layers separated. The organic phase, which contains the desired product and solvent mixture, was washed with water and treated under argon with 25 grams of alumina. After the alumina was filtered off, the organic phase was evaporated to remove most of the toluene. The above product was obtained by recrystallization of the residue from cyclohexane. Yield: 6.8 grams. IR (Kbr): 1,604, 1,588, 1,490, 1,475, 1,450, 1,321, 1,201, 1,153, 760, 745, 701 cm-1. 1H-NMR (CDCl3): δ2.51 (s), 7.18-7.59 (m), 8.05 (s), 8.12 (d, J=8.5 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05942340
출처 데이터셋uspto-grants-1999_08
ORD IDord-06141d4b92b945838bbed33f947a8737
출처 메모uspto-grants-1999_08