関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2,5-Dichlorobenzonitrile | HCID 89000 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-Chloro-2-(2,2,2-trifluoroethoxy)benzonitrile | HCID 19075161 | 59.4% |
反応手順
Under a nitrogen atmosphere, in a round-bottom flask were placed 880 mg (22mmol) of 60% sodium hydride (NaH) and 12 ml of N,N-dimethylformamide. To the system were added 2.9 ml (4 g, 40 mmol) of 2,2,2-trifluoroethanol via syringe over a period of 15 minutes and the mixture was stirred at room temperature for 20 minutes. To the system were added 1.72 g (10 mmol) of 2,5-dichlorobenzonitrile, and the mixture was heated at 90° C. for three days. The mixture was cooled to room temperature, poured into 50 ml of 2M aqueous HCl and extracted with three portions of ether. The combinedorganic fractions were dried (Na2SO4) and concentrated to afford2.5 g of a solid. The crude material was purified by flash column chromatography using 1:49 ethyl acetate/hexanes as the eluant to obtain 1.4 g of 5-chloro-2-(2,2,2-trifluoroethoxy)benzonitrile as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05744480 |
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| 出典データセット | uspto-grants-1998_04 |
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| ORD ID | ord-1c685416802548d48842b7b9fa2acd33 |
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| 出典メモ | uspto-grants-1998_04 |
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