関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Pyridiniumtribromide | HCID 21124087 | — |
| 反応物 | 4-(3-Bromo-phenyl)-1H-indole | HCID 22561906 | — |
| 触媒 | Zinc | HCID 23994 | — |
| 溶媒 | t-BuOH ethanol aceticacid | HCID 86587657 | — |
| 生成物 | 4-(3-Bromo-phenyl)1,3-dihydro-indol-2-one | HCID 22561849 | 65% |
反応手順
To the suspension of 4-(3-bromo-phenyl)-1H-indole (1.48 g, 5.44 mmol) in t-BuOH-ethanol-acetic acid (3:2:1) (66 mL) was added pyridinium tribromide (90% purity from Aldrich, 5.80 g, 16.3 mmol)) portionwise. The mixture was stirred at 27° C. for 3 hours, and then to the mixture was added acetic acid (26 mL). Zinc dust was added to the reaction mixture portionwise until the color changed from deep red to light yellow, and the reaction mixture was stirred at room temperature for one hour. The unreacted zinc dust was filtered off and washed with ethanol. The filtrate was concentrated, and the syrupy residue was dissolved in ethyl acetate, which was washed with water, 0.5 N HCl, sat. NaHCO3 and brine, and dried over Na2SO4. After filtration and evaporation, the crude product was triturated with diethyl ether to provide product 4-(3-bromo-phenyl)-1,3-dihydro-indol-2-one (1.02 g, 65%) as a tan solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06861418B2 |
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| 出典データセット | uspto-grants-2005_03 |
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| ORD ID | ord-fa5c429054d34c36a1b1d6e08887fb8e |
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| 出典メモ | uspto-grants-2005_03 |
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