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HRID 383477생성일: 2026년 10월 26일

6-fluoro-2,3-dihydro-1H-indol-2-one → 3-(4-bromo-5H-furan-2-ylidene)-6-fluoro-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/383477

반응식

참여 물질

역할이름HCID투입량
반응물6-fluoro-2,3-dihydro-1H-indol-2-oneHCID 3731013—
반응물4-bromo-5H-furan-2-oneHCID 11789536—
반응물LiHMDS tetrahydrofuranHCID 23714775—
용매TetrahydrofuranHCID 8028—
생성물3-(4-bromo-5H-furan-2-ylidene)-6-fluoro-1,3-dihydro-indol-2-oneHCID 69401889—

반응 조건

온도0 °C

반응 단계

To a 0° C. stirred solution of 6-fluorooxindole (370 mg, 2.45 mmol) in anhydrous THF (10 mL) was added 1M LiHMDS/THF solution (4.9 mL, 4.9 mmol). The mixture was stirred at 0° C. for 10 minutes. 4-Bromo-5H-furan-2-one (200 mg, 1.23) was added as a solution in 2 mL of THF. The resulting mixture was stirred at 0° C. for 30 minutes, then at room temperature for 1 hour and quenched with 10 mL of 2M HCl. Methanol (5 mL) was added and the mixture was stirred at 50° C. for 0.5 hour. The mixture was poured into 150 mL of water and then stirred for 30 minutes. The precipitates were filtered, washed with water, and dried in vacuum to give 3-(4-bromo-5H-furan-2-ylidene)-6-fluoro-1,3-dihydro-indol-2-one as a yellow solid. Yield: 228 mg, 63%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367664B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-ea051f6b120a48f1baf1202b2458ae29
출처 메모uspto-grants-2013_02