참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diiodomethane | HCID 6346 | — |
| 반응물 | 3-Cyanophenol | HCID 13394 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 6-Nitro-1H-indole | HCID 78502 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrile | HCID 90030447 | 51% |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434695B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-4ac7af751afe4a0c8814018ded4486d1 |
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| 출처 메모 | uspto-grants-2016_09 |
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