化工社化工社 化学情報印刷レポート · 研究参考用
3-Hydroxyacetophenone → 1-[3-(3-Phenylpropoxy)phenyl]ethan-1-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Hydroxyacetophenone | HCID 8487 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | (3-Bromopropyl)benzene | HCID 12503 | — |
| 触媒 | Sodium Iodide | HCID 5238 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-[3-(3-Phenylpropoxy)phenyl]ethan-1-one | HCID 21422440 | 94.4% |
反応手順
3′-Hydroxyacetophenone (6.81 g, 50 mmol) and 1-bromo-3-phenyl propane (11.95 g, 60 mmol) were dissolved in dimethylformamide (70 ml). Then, potassium carbonate (15 g) and sodium iodide (0.5 g) were added thereto and the mixture was allowed to react for 7 hours at 80° C. Ethyl acetate (300 ml) and purified water (200 ml) were further added to the reaction mixture prior to stirring for 30 min. The organic layer extracted with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:5) to obtain the title compound (12.0 g, yield 94.2%) as a gel.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07741323B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-4521dbc84ec14ce1a4ca820a0481d911 |
| 出典メモ | uspto-grants-2010_06 |