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Methanol → potassium 2-(4-(1H-pyrazol-1-yl)phenyl)-2-methoxyacetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Bromoform | HCID 5558 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 4-(1H-Pyrazol-1-yl)benzaldehyde | HCID 2776477 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | potassium 2-(4-(1H-pyrazol-1-yl)phenyl)-2-methoxyacetate | HCID 67388986 | — |
反応手順
To a stirred solution of 4-(1H-pyrazol-1-yl)benzaldehyde (1.3 g, 7.55 mmol) and bromoform (0.85 mL, 9.75 mmol) in MeOH (10 mL) and dioxane (10 mL) was added dropwise a solution of potassium hydroxide (2.2 g, 39 mmol) in MeOH (10 mL) over 15 minutes. Stirring was then continued for 23 hours. The mixture was filtered through Celite, rinsed through with EtOAc and concentrated under reduced pressure to yield potassium 2-(4-(1H-pyrazol-1-yl)phenyl)-2-methoxyacetate as a light yellow solid (3.2 g) that was used without further purification. See U.S. Pat. No. 7,129,238.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09434707B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-034ed94b6f7243d68a696cd0661a86e9 |
| 出典メモ | uspto-grants-2016_09 |