関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1-(2-Bromoethyl)-4-chlorobenzene | HCID 23029 | — |
| 反応物 | 3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidine | HCID 22853758 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1-(4-chlorophenethyl)-3-(R)-(+)-(1-cyano-1,1diphenylmethyl)piperidine | HCID 22853752 | — |
反応手順
A mixture containing 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)piperidine (1 g--see Preparation 1), 4-chlorophenethyl bromide (0.72 g), anhydrous potassium carbonate (1.5 g) and acetonitrile (25 ml) was heated under reflux for 4 hours. The mixture was partitioned between dichloromethane (50 ml) and 10% aqueous potassium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (3×30 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give an oil which was purified by column chromatography on silica eluting with hexane containing dichloromethane (30% up to 70%) and then dichloromethane containing methanol (0% up to 5%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from acetonitrile to give the title compound as colourless rhombs, yield 0.85 g, m.p. 129°14 131° C. [α]D25 +20.3 (c 1.0, CH2Cl2)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05422358 |
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| 出典データセット | uspto-grants-1995_06 |
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| ORD ID | ord-dd99be49ecbc46eba4904d687e239f52 |
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| 出典メモ | uspto-grants-1995_06 |
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