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Sodium Hydroxide → 3-Methyl-4-(1,3-oxazol-4-yl)phenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Ammonium formate | HCID 2723923 | — |
| 反応物 | 2-Bromo-1-(4-hydroxy-2-methylphenyl)ethanone | HCID 17812170 | — |
| 溶媒 | Formic Acid | HCID 284 | — |
| 生成物 | 3-Methyl-4-(1,3-oxazol-4-yl)phenol | HCID 22316743 | 13.2% |
反応手順
A mixture of 2-bromo-1-(4-hydroxy-2-methylphenyl)-1-ethanone (18 g, 78 mmol), ammonium formate (17 g, 273 mmol) in formic acid (100 ml) was heated at reflux temperature for 3 hours. The mixture was cooled down to room temperature and made basic by addition of 50% NaOH aqueous solution at 0° C. The whole was extracted with CH2Cl2. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate-hexane (1:5) to give title compound (1.8 g, 13% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06294558B1 |
| 出典データセット | uspto-grants-2001_09 |
| ORD ID | ord-64e4b705c3314c3e991c17ce854b50c3 |
| 出典メモ | uspto-grants-2001_09 |