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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
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-carboxylate | HCID 2773516 | — |
| 反応物 | 4-Bromo-5,5-dimethylfuran-2-one | HCID 12671960 | — |
| 反応物 | LiHMDS tetrahydrofuran | HCID 23714775 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | methyl (3E)-3-(4-bromo-5,5-dimethylfuran-2(5H)-ylidene)-2-oxoindoline-5-carboxylate | HCID 58926238 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08877923B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-557b12f398bb4a36a7b59188670d8f55 |
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| 出典メモ | uspto-grants-2014_11 |
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