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Diisopropylamine → N-(1-Hydroxy-1-phenylprop-2-yl)-N-methyl-2-butyl-3-cyclohexylpropionamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropylamine | HCID 7912 | — |
| 反応物 | Butyl iodide | HCID 10962 | — |
| 反応物 | Lithium Chloride | HCID 433294 | — |
| 反応物 | N-(1-Hydroxy-1-phenylprop-2-yl)-N-methyl-3-cyclohexylpropionamide | HCID 22014104 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 生成物 | N-(1-Hydroxy-1-phenylprop-2-yl)-N-methyl-2-butyl-3-cyclohexylpropionamide | HCID 22014296 | 53% |
反応手順
A solution of 2.5M nBuLi in hexanes (5.8 mL, 14.5 mmol), diisopropylamine (2.0 mL, 14.5 mmol), lithium chloride (1.6 g, 39 mmol), iodobutane (130 μL, 6.4 mmol) and the product from Example 1315A (2.0 g, 6.4 mmol) were allowed to react in a manner similar to that described by A. G. Myers et al., Journal of the American Chemical Society 1994, 116: 9361-9362. The crude residue was chromatographed (silica gel; EtOAc/hexanes, 1:4) to afford the title compound as a yellow oil (1.2 g, 53%). MS (CI/NH3) m/z: 360 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06204293B1 |
| 出典データセット | uspto-grants-2001_03 |
| ORD ID | ord-6e05987e8b25483c86f021efc43c34e7 |
| 出典メモ | uspto-grants-2001_03 |