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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

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 2,3-dihydro-2-oxo-1H-indole-5-carboxylateHCID 2773516—
반응물4-Bromo-5,5-dimethylfuran-2-oneHCID 12671960—
반응물LiHMDS tetrahydrofuranHCID 23714775—
용매TetrahydrofuranHCID 8028—
생성물methyl (3E)-3-(4-bromo-5,5-dimethylfuran-2(5H)-ylidene)-2-oxoindoline-5-carboxylateHCID 58926238—

반응 조건

온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367664B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-b0204de75f414848aed1d1e509ad7d62
출처 메모uspto-grants-2013_02