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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400691생성일: 2026년 10월 26일

1,5,6,7-Tetrahydro-4H-indol-4-one → 1-[4-(2,3-Dihydrobenzofuran-7-yl)-2-hydroxy-4-methyl-2-trifluoromethylpentyl]-1,5,6,7-tetrahydroindol-4-one

https://huagongshe.com/reaction/400691

반응식

참여 물질

역할이름HCID투입량
반응물1,5,6,7-Tetrahydro-4H-indol-4-oneHCID 280229—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium ethoxideHCID 2723922—
반응물7-[1,1-Dimethyl-2-(2-trifluoromethyloxiranyl)ethyl]-2,3-dihydrobenzofuranHCID 57775518—
용매EthanolHCID 702—
생성물1-[4-(2,3-Dihydrobenzofuran-7-yl)-2-hydroxy-4-methyl-2-trifluoromethylpentyl]-1,5,6,7-tetrahydroindol-4-oneHCID 6002642366%

반응 조건

온도85 °C

반응 단계

To a suspension of 7-[1,1-dimethyl-2-(2-trifluoromethyloxiranyl)ethyl]-2,3-dihydrobenzofuran (59.2 mg, 0.21 mmol) and 1,5,6,7-tetrahydroindol-4-one (56.0 mg, 0.41 mmol) in 0.4 mL of anhydrous ethanol was added 0.077 mL of sodium ethoxide solution (21 wt % in ethanol). The reaction mixture was then heated at 85° C. for 16 hours. The resulting mixture was poured into half-saturated sodium bicarbonate and extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (eluted with 35% ethyl acetate-hexanes) to give 58.4 mg (66% yield) of the title compound as a white solid, m.p. 145° C.-146° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741897B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-b077ed2160254a968b0fff0f79d3f0f8
출처 메모uspto-grants-2014_06