関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 反応物 | 2-(4-Chloropyridin-2-yl)-1-(4-fluorophenyl)ethan-1-one | HCID 21874061 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2-(4-Chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime | HCID 73851753 | 84% |
反応手順
To a solution of 2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone (9.6 g, 38 mmol) in methanol (200 mL) was added hydroxylamine hydrochloride (13.5 g, 190 mmol) followed by the addition of a sodium hydroxide solution (7.8 g, 190 mmol in 50 mL of water). The resulting suspension was heated at reflux for 2 hours and then allowed to cool to room temperature. The mixture was concentrated and water was added to the resulting slurry. A white precipitate formed, which was collected by filtration, washed with water and dried (magnesium sulfate) to give 2-(4-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime (8.45 g, 84%) as a white solid. 1H-NMR (DMSO-d6): δ 11.56 (s, 1H), 8.44 (d, 1H), 7.80 (m, 2H), 7.40 (m, 2H), 7.22 (m, 2H), 4.29 (s, 2H); 19F-NMR (DMSO-d6): δ −113.44; MS m/265 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07141569B2 |
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| 出典データセット | uspto-grants-2006_11 |
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| ORD ID | ord-b8a24a5ac03f421faaf73b618c491709 |
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| 出典メモ | uspto-grants-2006_11 |
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