関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl iodide | HCID 6328 | — |
| 反応物 | Cyclohexane | HCID 8078 | — |
| 反応物 | Benzeneacetonitrile, 4-methoxy- | HCID 66031 | — |
| 反応物 | 2-(4-Methoxyphenyl)-2-methylpropanenitrile | HCID 219166 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | 2-(4-Ethoxyphenyl)propanenitrile | HCID 13254522 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ammonium Chloride | HCID 25517 | — |
| 生成物 | 2-(4-Methoxyphenyl)-2-methylpropan-1-amine | HCID 3581364 | 33% |
反応手順
To a solution of (4-methoxy-phenyl)-acetonitrile [5 g, 34 mmol] in THF (40 mL), is added a 1.5 M solution of lithium diisopropylamide in cyclohexane (36 mL, 54 mmol) at −78° C. After 2 hours at −78° C., methyl iodide (3.4 g, 54 mmol) is added, and the mixture is allowed to warm to room temperature over 3 hours. After additional 12 hours at 20° C., the mixture is diluted with aqueous ammonium chloride solution, and extracted with ethyl acetate. The extracts are dried over magnesium sulfate, filtered and concentrated. The residue is subjected to chromatography on silica gel eluting with 40% EtOAc in heptane to afford a mixture of 2-(4-ethoxy-phenyl)-propionitrile and 2-(4-methoxy-phenyl)-2-methyl-propionitrile. To above mixture (5 g) in THF (20 mL) is add a 2 M solution of lithium aluminum hydride (35 mL, 70 mmol) at 0° C. After 12 hours at 20° C., the mixture is carefully quenched with 10% sodium hydroxide solution, and the white slurry is diluted with ether. The mixture is dried over magnesium sulfate, filtered and concentrated. The residue is subjected to chromatography on silica to afford 2-(4-methoxy-phenyl)-2-methyl-propylamine [2 g, 33%, Intermediate (35)]. MS: 180 (M+H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08193183B2 |
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| 出典データセット | uspto-grants-2012_06 |
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| ORD ID | ord-a2e8851f2c1d4f27b7ceaa176f8c7208 |
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| 出典メモ | uspto-grants-2012_06 |
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