関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Cyanide | HCID 8929 | — |
| 反応物 | Acetonitrile, fluoro- | HCID 10420 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 1-Chloro-3-methoxypropane | HCID 118927 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-Amino-2-(fluoromethyl)-5-methoxypentanenitrile | HCID 19966334 | 99.9% |
| 生成物 | HCID 178495109 | HCID 178495109 | — |
反応手順
Under an atmosphere of nitrogen, 3-methoxypropyl magnesium chloride is prepared from 3-methoxy-1-chloropropane (5.43 g, 50 mmol), prepared according to Haworth and Perkin, Chem. Zentralblatt, II, 1271 (1912) and magnesium turnings (1.22 g, 50 mmol) in dry THF (50 ml). The mixture is heated under reflux for 3 hours, then cooled to -30° C. and a solution of fluoroacetonitrile (2.95 g, 50 mmol) in THF (30 ml) is added during 20 minutes. After keeping the mixture at -30° C. for 1/2 hour more, a solution of sodium cyanide (4.9 g, 100 mmol) and ammonium chloride (8.09 g, 150 mmol) in water (100 ml), previously cooled to 0° C., is added and the mixture is stirred for 3/4 hour at room temperature. After saturating with sodium chloride, the THF layer is separated and the aqueous phase is extracted twice with ether. After drying (Na2SO4), the combined organic extracts are evaporated to give 2-fluoromethyl-2-amino-5-methoxypentanenitrile (4.0 g) as a brown oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04743691 |
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| 出典データセット | uspto-grants-1988_05 |
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| ORD ID | ord-2b7703a477ff49669e7de67f7572a85c |
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| 出典メモ | uspto-grants-1988_05 |
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