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Dimethylformamide → 6-(2-Pyridyl)-methyloxy-2-acetylnaphthalene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Picolyl chloride hydrochloride | HCID 23392 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 1-(6-Hydroxy-2-naphthyl)ethan-1-one | HCID 82631 | — |
| 生成物 | 6-(2-Pyridyl)-methyloxy-2-acetylnaphthalene | HCID 23356934 | 75.5% |
反応手順
To a solution of 6-hydroxy-2-acetylnaphthalene (1.04 g) in DMF (20 ml) were added sodium hydride (60%, 0.65 g) and 2-picolyl chloride hydrochloride (1.28 g) under ice-cooling and the resultant-mixture was stirred at room temperature for 12 hours. The reaction mixture was partitioned between toluene and water. The organic layer was washed with a saturated saline solution and dried over anhydrous magnesium sulfate. After concentration in vacuo, the residue was subjected to column chromatography on silica gel eluting with ethyl acetate/hexane to obtain the title compound (1.17 g, yield =75.5%). The NMR spectrum is as follows.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05594016 |
| 出典データセット | uspto-grants-1997_01 |
| ORD ID | ord-2f56598a329a4ed4b113a669773b9a55 |
| 出典メモ | uspto-grants-1997_01 |