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HRID 2102653생성일: 2026년 10월 25일

5-chloro-1H-indole-2,3-dione → 5-Chloro-3-hydroxy-3-(4-methoxyphenyl)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/2102653

반응식

참여 물질

역할이름HCID투입량
반응물5-chloro-1H-indole-2,3-dioneHCID 87203—
반응물HCID 178491912HCID 178491912—
용매TetrahydrofuranHCID 8028—
생성물5-Chloro-3-hydroxy-3-(4-methoxyphenyl)-1,3-dihydro-2H-indol-2-oneHCID 22560907—

반응 조건

온도-25 °C

반응 단계

A solution of 4-methoxyphenyl magnesium bromide in tetrahydrofuran (0.5 M, 50 mL, 25 mmol) (Aldrich) was added dropwise to a suspension of 5-chloroisatin (1.82 g, 10 mmol) (Avocado) in tetrahydrofuran (20 mL) under argon with cooling in a −25° C. bath and magnetic stirring at such a rate that reaction temperature was kept below −10° C. (approximately 30 minutes). Cooling bath was then removed and mixture allowed to warm to room temperature. After stirring for an additional 1 hour, 15% aqueous ammonium chloride solution (50 mL) was added and mixture extracted with ethyl acetate (2×75 mL). Ethyl acetate layers were then washed with water (75 mL), brine (75 mL), combined, dried (MgSO4), filtered and concentrated. Residue was stirred in dichloromethane (100 mL) at room temperature for 30 minutes and filtered to give crude rac-5-chloro-3-hydroxy-3-(4-methoxy-phenyl)-1,3-dihydro-indol-2-one as a white powder. (Yield 2.57 g, 88.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07576082B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-91cda980f6434b6ea96b3b3d21a732a5
출처 메모uspto-grants-2009_08