참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Bromoacetonitrile | HCID 11534 | — |
| 반응물 | 7-Hydroxyindole | HCID 2737651 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 7-(Cyanomethoxy)indole | HCID 15054020 | — |
반응 단계
In a 100 mL roundbottom flask equipped with a magnetic stirrer and rubber septum, 7-hydroxy-1H-indole (1.66 g., 12.48 mmol) was dissolved 50 mL anhydrous acetonitrile. The flask was charged with potassium carbonate (6.88 g., 49.9 mmol) and cooled to 0° C. While stirring, bromoacetonitrile (1.64 g., 13.73 mmol) was added dropwise over two minutes. The reaction mixture was allowed to warm to ambient temperature and stirring was continued for three hours. The solution was washed with water (2×30 mL) and brine (1×30 mL), dried over MgSO4 and concentrated in vacuo. The resulting oily brown residue was purified by flash chromatography (95:5 ethyl acetate:hexanes to 85:15 ethyl acetate:hexanes over minutes) to give (1H-Indol-7-yloxy)-acetonitrile as a crystalline solid (0.244-g.) ms: (M−H)−=171.2.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07084169B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-586c518b04a74c998bdaf509414209bb |
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| 출처 메모 | uspto-grants-2006_08 |
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