참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Pyridiniumtribromide | HCID 21124087 | — |
| 반응물 | 4-(4-Methoxyphenyl)-1H-indole | HCID 22561940 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 용매 | t-BuOH ethanol aceticacid | HCID 86587657 | — |
| 생성물 | 4-(4-Methoxy-phenyl)-1,3-dihydro-indol-2-one | HCID 22561901 | 84% |
반응 단계
To the suspension of 4-(4-methoxy-phenyl)-1H-indole (1.84 g, 8.24 mmol) in t-BuOH-ethanol-acetic acid (3:2:1) (99 mL) was added pyridinium tribromide (90% purity from Aldrich, 8.78 g, 24.72 mmol)) portionwise. The mixture was stirred at 27° C. for 3 hours, and then to the mixture was added acetic acid (40 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-(4-methoxy-phenyl)-1,3-dihydro-indol-2-one (1.66 g, 84%) as a tan solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06861418B2 |
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| 출처 데이터셋 | uspto-grants-2005_03 |
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| ORD ID | ord-121babf6e6c74f92ba68c8998064dc26 |
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| 출처 메모 | uspto-grants-2005_03 |
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