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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,5,6,7-Tetrahydro-4H-indol-4-one | HCID 280229 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Sodium ethoxide | HCID 2723922 | — |
| 반응물 | 7-[1,1-Dimethyl-2-(2-trifluoromethyloxiranyl)ethyl]-2,3-dihydrobenzofuran | HCID 57775518 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-[4-(2,3-Dihydrobenzofuran-7-yl)-2-hydroxy-4-methyl-2-trifluoromethylpentyl]-1,5,6,7-tetrahydroindol-4-one | HCID 60026423 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08741897B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-b077ed2160254a968b0fff0f79d3f0f8 |
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| 출처 메모 | uspto-grants-2014_06 |
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