돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333377생성일: 2026년 10월 25일

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/reaction/333377

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 번호US08877923B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-557b12f398bb4a36a7b59188670d8f55
출처 메모uspto-grants-2014_11