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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2196128생성일: 2026년 10월 25일

(+-)-3-Methyl-2,4(3H,5H)-furandione → 6-fluoro-3-(4-methoxy-5H-furan-2-ylidene)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/2196128

반응식

참여 물질

역할이름HCID투입량
반응물(+-)-3-Methyl-2,4(3H,5H)-furandioneHCID 544553—
반응물6-fluoro-2,3-dihydro-1H-indol-2-oneHCID 3731013—
반응물LiHMDS tetrahydrofuranHCID 23714775—
용매TetrahydrofuranHCID 8028—
생성물6-fluoro-3-(4-methoxy-5H-furan-2-ylidene)-1,3-dihydro-indol-2-oneHCID 69401606—

반응 단계

To a stirred solution of 6-fluorooxindole (2.6 g, 17.5 mmol) in anhydrous THF (30 mL) under nitrogen was added 1.0M LiHMDS/THF solution (35 mL, 35 mmol). The mixture was stirred at room temperature for 10 minutes. Methyl tetronate (1.0 g, 8.8 mmol) was added as one portion. After stirring at room temperature for 1 hour, the reaction was cooled to 0° C., and quenched with 2M HCl until pH=3. The mixture was stirred at room temperature for 2 more hours, and poured into 250 mL of water. The resulting precipitates were filtered, rinsed with water and dried in vacuum to give 6-fluoro-3-(4-methoxy-5H-furan-2-ylidene)-1,3-dihydro-indol-2-one as off-white solid. Yield: 840 mg, 38%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08338415B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-a6928e0ca5b8442a8da9a296788aa034
출처 메모uspto-grants-2012_12