Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383496생성일: 2026년 10월 24일
Methyl 2,3-dihydro-2-oxo-1H-indole-5-carboxylate → methyl (3E)-3-(4-bromo-5,5-dimethylfuran-2(5H)-ylidene)-2-oxoindoline-5-carboxylate
https://huagongshe.com/ko/reaction/383496
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methyl 2,3-dihydro-2-oxo-1H-indole-5-carboxylate | HCID 2773516 | — |
| 반응물 | 4-Bromo-5,5-dimethylfuran-2-one | HCID 12671960 | — |
| 반응물 | LiHMDS tetrahydrofuran | HCID 23714775 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | methyl (3E)-3-(4-bromo-5,5-dimethylfuran-2(5H)-ylidene)-2-oxoindoline-5-carboxylate | HCID 58926238 | — |
반응 단계
To a 0° C. stirred solution of methyl oxindole-5-carboxylate (421 mg, 2.2 mmol) and 4-bromo-5,5-dimethylfuran-2(5H)-one (382 mg, 2.0 mmol) in THF (10 mL), was added 1M LiHMDS/THF solution (4.4 mL, 4.4 mmol) under nitrogen. The mixture was stirred at 0° C. for 80 min, quenched with 2.5M H2SO4 (3 mL), and poured into 100 mL of water. The precipitates were filtered, washed with water, and dried in vacuo to give methyl (3E)-3-(4-bromo-5,5-dimethylfuran-2(5H)-ylidene)-2-oxoindoline-5-carboxylate as yellow solid. Yield: 408 mg, 56%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08367664B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-b0204de75f414848aed1d1e509ad7d62 |
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| 출처 메모 | uspto-grants-2013_02 |
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