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HRID 2050513생성일: 2026년 10월 24일

Iodoethane → 4-Ethyl-8-(3-(trifluoromethyl)phenyl)-3H,6H-1,4,5a,8a-tetraazaacenaphthylene-3,5(4H)-dione

https://huagongshe.com/ko/reaction/2050513

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Sodium hydrideHCID 24758—
반응물8-(3-(Trifluoromethyl)phenyl)-3H,6H-1,4,5a,8a-tetraazaacenaphthylene-3,5(4H)-dioneHCID 15044076—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
생성물4-Ethyl-8-(3-(trifluoromethyl)phenyl)-3H,6H-1,4,5a,8a-tetraazaacenaphthylene-3,5(4H)-dioneHCID 20058375—

반응 단계

To a stirred mixture of 5.0 g of 8-(3-(trifluoromethyl)phenyl)-3H,6H-1,4,5a,8a-tetraazaacenaphthylene-3,5(4H)-dione (prepared as described in Example 14) in 50 ml of dry N,N-dimethylformamide, under nitrogen, is added 800 mg of 60 percent sodium hydride (dispersion in mineral oil). The mixture is stirred at room temperature for 2 hours, then 10 ml of iodoethane is added and stirring is continued for 48 hours. The reaction mixture is evaporated to dryness, then treated with water, and the gummy solid which is isolated is dissolved in chloroform and the extract dried over anhydrous sodium sulfate. Evaporation gives an oil which is triturated with diethyl ether-hexane to provide a yellow solid which is collected by filtration to give 2.0 g of the desired product as a white solid. The product is recrystallized from isopropyl alcohol, mp 161-163° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05013737
출처 데이터셋uspto-grants-1991_05
ORD IDord-29f8a411b7dd4c85a46fb10dcf333c92
출처 메모uspto-grants-1991_05