Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 5-chloro-1H-indole-2,3-dione | HCID 87203 | — |
| 반응물 | HCID 178491912 | HCID 178491912 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Chloro-3-hydroxy-3-(4-methoxyphenyl)-1,3-dihydro-2H-indol-2-one | HCID 22560907 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07576082B2 |
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| 출처 데이터셋 | uspto-grants-2009_08 |
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| ORD ID | ord-91cda980f6434b6ea96b3b3d21a732a5 |
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| 출처 메모 | uspto-grants-2009_08 |
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