関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cyanide | HCID 5975 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | HCID 178418689 | HCID 178418689 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 1,1'-Bipiperidine | HCID 68279 | 79% |
反応手順
The cyanide (4.87 g, 15 mmol) was taken up in THF (75 ml). CH3MgBr (25 ml of a 3.0 M solution in Et2O) was added to the reaction mixture at 0° C. The solution was allowed to warm to 25° C. and was stirred at that temperature for 18 h. The solution was partitioned between 25 wt % aqueous solution of sodium citrate and EtOAc. The aqueous layer was extracted with EtOAc. The combined EtOAc layers were washed with brine and dried (Na2SO4). Filtration and concentration gave a yellow oil. Purification via flash chromatography (95/5 to 90/10 EtOAc/MeOH. SiO2) gave 3.7 g (79%) of the piperidino-piperidine 12 as a yellow gum.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07098213B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-70419371049d4118a56e44f216f0f529 |
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| 出典メモ | uspto-grants-2006_08 |
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