関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diiodomethane | HCID 6346 | — |
| 反応物 | 3-Cyanophenol | HCID 13394 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 6-Nitro-1H-indole | HCID 78502 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrile | HCID 90030447 | 51% |
反応手順
To a mixture of NaH (3.0 g, 75.0 mmol, 60%) in DMF (20 mL) were added a solution of 6-nitro-1H-indole (4.86 g, 30.0 mmol) in DMF (10 mL) and a solution of 3-hydroxybenzonitrile (3.57 g, 30.0 mmol) in DMF (10 mL) at 0° C. and the mixture was stirred at rt for 2 h. To the reaction mixture was added a solution of diiodomethane (7.5 mL, 90.0 mmol) in DMF (10 mL) slowly without light and the mixture was stirred at rt for 20 h. The mixture was then quenched with water and filtered. The filtrate was extracted with DCM (30 mL×6) and the combined organic layers were washed with brine (50 mL×3), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a yellow solid (4.47 g, 51%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09434695B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-4ac7af751afe4a0c8814018ded4486d1 |
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| 出典メモ | uspto-grants-2016_09 |
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