関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Benzene, (2-bromoethoxy)- | HCID 68526 | — |
| 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-(2-phenoxyethyl)piperidine | HCID 22853753 | — |
反応手順
A mixture containing 3-(R)-(1-cyano-1,1-diphenylmethyl)piperidine (0.3 g), 2-phenoxyethyl bromide (0.24 g--commercially available), anhydrous potassium carbonate (0.5 g) and acetonitrile (15 ml) was heated under reflux for 5 hours. The mixture was then partitioned between dichloromethane (30 ml) and 10% aqueous potassium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (2×20 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give a gum which was purified by column chromatography on silica eluting with dichloromethane containing methanol (0% up to 2%). The product-containing fractions were combined and concentrated in vacuo to give the title compound as a gum, yield 0.254 g.
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-ea33f5fb19be4a2b81c7fb2b7aa97c11 |
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| 出典メモ | uspto-grants-1995_06 |
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