関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | (2S)-2-[(5-Fluoro-2-nitrophenoxy)methyl]oxirane | HCID 28109166 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Platinum | HCID 23939 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | N-{4-Fluoro-2-[(2S)-oxiran-2-ylmethoxy]phenyl}acetamide | HCID 20806548 | 61.3% |
反応手順
(2S)-2-[(5-fluoro-2-nitrophenoxy)methyl]oxirane (0.32 g, 1.5 mmol) was dissolved in ethyl acetate (40 ml). Platinum on charcoal (0.15 g) was added, and the mixture was stirred in the atmosphere of hydrogen for 3 h at room temperature and atmospheric pressure. The catalyst was filtered and washed on the filter with ethyl acetate (10 ml). Acetic anhydride (0.31 g, 0.28 ml, 3 mmol) and ethyldi(i-propyl)amine (0.39 g, 0.52 ml, 3 mmol) were added to the solution. The reaction mixture was stirred at room temperature for 3 h, then washed with 1M sodium hydroxide (NaOH) (30 ml) and brine (30 ml), and dried with sodium sulphate (Na2SO4). Evaporation of the solvent and flash chromatography on silica gel with n-heptane/ethyl acetate (from 25 to 75%) afforded the subtitle compound (0.21 g, 0.92 mmol, 61%) as a colourless solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07388020B2 |
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| 出典データセット | uspto-grants-2008_06 |
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| ORD ID | ord-f285811dac3e41b995ef2461e620a5c0 |
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| 出典メモ | uspto-grants-2008_06 |
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