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HRID 333377作成日:2026年10月24日

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/ja/reaction/333377

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2,3-dihydro-2-oxo-1H-indole-5-carboxylateHCID 2773516—
反応物4-Bromo-5,5-dimethylfuran-2-oneHCID 12671960—
反応物LiHMDS tetrahydrofuranHCID 23714775—
溶媒TetrahydrofuranHCID 8028—
生成物methyl (3E)-3-(4-bromo-5,5-dimethylfuran-2(5H)-ylidene)-2-oxoindoline-5-carboxylateHCID 58926238—

反応条件

温度0 °C

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08877923B2
出典データセットuspto-grants-2014_11
ORD IDord-557b12f398bb4a36a7b59188670d8f55
出典メモuspto-grants-2014_11