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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15268생성일: 2026년 10월 26일

Water → 5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dione

https://huagongshe.com/reaction/15268

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물4-Methyloxybenzyl chlorideHCID 69993—
반응물5-FluoroisatinHCID 236566—
용매DimethylformamideHCID 6228—
용매Ethyl acetate hexaneHCID 21226206—
생성물5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dioneHCID 767710080%

반응 단계

5-Fluoro-1H-indole-2,3-dione (956 mg, 5.79 mmol, 1 eq) was added as a solution in dry DMF to a stirred slurry of sodium hydride (278 mg, 11.6 mmol, 2 eq) in dry DMF drop wise over 15 minutes under an inert atmosphere with adequate pressure release to accommodate H2 evolution. The resulting mixture was stirred for 1 hour and p-methoxybenzyl chloride was added via syringe to the reaction. The solution was then stirred ca 2 hours and worked up by addition of water followed by extraction into ethyl acetate. The organic layer was washed twice with water and then dried over MgSO4. Column chromatography with ethyl acetate/hexane afforded 5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione as a red solid (1.3 g, 80% yield). 1H NMR (CDCl3) δ (ppm): 7.3-7.24 (m, 3H), 7.20 (td, J=8.7, 2.7 Hz, 1H), 6.9-6.86 (m, 2H), 6.76 (dd, J=8.6, 3.6 Hz, 1H), 3.81 (s, 2H), 3.78 (s, 3H). LC/MS=286.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732449B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-dbc008b6d4344431a0479a5e6a29980f
출처 메모uspto-grants-2010_06