関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Hydrogen Peroxide | HCID 784 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 2-Methoxy-5-(trifluoromethoxy)benzaldehyde | HCID 2783364 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2-methoxy-5-(trifluoromethoxy)benzoic Acid | HCID 2775286 | 91% |
反応手順
To a stirred solution of 2-methoxy-5-trifluoromethoxybenzaldehyde (2.0 g, 9.09 mmol) and 50% KOH (4.1 ml) in MeOH (15 ml) at 65° C. was added dropwise hydrogen peroxide (30%, 7.4 ml) over 20 min. The reaction mixture was then stirred at 65° C. for 10 min., cooled to room temperature, acidified with 1 M HCl, and extracted with Et2O (3×40 ml). The combined organic extracts were washed with brine (35 ml), dried (Na2SO4) and the solvent removed under reduced pressure to give a pale yellow viscous oil which solidified at room temperature overnight to give the title compound (1.95 g, 91%) as a pale yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08895313B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-42d02c996db540dcaa03b8c4c3c23326 |
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| 出典メモ | uspto-grants-2014_11 |
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