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Salicylaldehyde → Benzofuran-2-yl-(5-methyl-3-phenyl-isoxazol-4-yl)-methanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Salicylaldehyde | HCID 6998 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-(Bromoacetyl)-5-methyl-3-phenylisoxazole | HCID 2735531 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Benzofuran-2-yl-(5-methyl-3-phenyl-isoxazol-4-yl)-methanone | HCID 69106966 | 86% |
反応手順
To a solution of 4-(bromoacetyl)-5-methyl-3-phenylisoxazole (commercially available) (140 mg, 0.5 mmol) in DMF (0.5 mL) was added salicylaldehyde (61 mg, 53 μL, 0.5 mmol) followed by potassium carbonate (138 mg, 1.0 mmol) and the resulting mixture stirred vigorously at room temperature for 2 h. The mixture was then poured onto ice-water, and extracted with ethyl acetate. The combined organic layers were then washed with water and brine, dried over Na2SO4 and evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate:=100:0 to 1:1) afforded the title compound (131 mg, 86%) as a white solid. MS m/e: 304.0 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07388025B2 |
| 出典データセット | uspto-grants-2008_06 |
| ORD ID | ord-4379a3071e2943828002ed1f4588bafc |
| 出典メモ | uspto-grants-2008_06 |