関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-Hydroxy-3-methoxyphenethyl chloride | HCID 21224092 | — |
| 反応物 | 3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidine | HCID 22853758 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-(R)-(1-cyano-1,1-diphenylmethyl)-1-(4-hydroxy-3-methoxyphenethyl)piperidine | HCID 21311313 | — |
反応手順
A mixture containing 3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidine (0.3 g), 4-hydroxy-3-methoxyphenethyl chloride (0.233 g--see Preparation 6), anhydrous potassium carbonate (0.5 g), potassium iodide (0.2 g) and acetonitrile (15 ml) was heated under reflux for 5 hours. The mixture was partitioned between dichloromethane (40 ml) and 10% aqueous potassium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (2×30 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give a foam which was purified by column chromatography on silica eluting with dichloromethane containing methanol (5%). The product-containing fractions were combined and concentrated in vacuo to give a gum which was crystallised from acetonitrile to give the title compound as colourless rhombs, yield 0.132 g, m.p. 159-160°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05932594 |
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| 出典データセット | uspto-grants-1999_08 |
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| ORD ID | ord-373af05fa05342b88789b4e63b48caab |
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| 出典メモ | uspto-grants-1999_08 |
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