関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Benzyl Bromide | HCID 7498 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 4-Cyanopiperidine | HCID 138223 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 溶媒 | Cyclohexane | HCID 8078 | — |
| 生成物 | 1,4-Dibenzyl-4-cyanopiperidine | HCID 22741742 | — |
反応手順
A solution of 15 g of 4-cyanopiperidine in 250 ml of THF is cooled to -50° C., 190 ml of a 1.5M solution of lithium diisopropylamide in cyclohexane are added dropwise and the mixture is stirred for 30 minutes at -50° C. 34 ml of benzyl bromide are then added and the mixture is stirred for 3 hours after the temperature has been allowed to rise to RT. The reaction mixture is poured into an ice/concentrated HCl mixture, ether is added and the precipitate formed is filtered off and washed with water. The precipitate is taken up with water, rendered alkaline to pH 12 by the addition of concentrated NaOH solution, and extracted with ether, the organic phase is dried over MgSO4 and the solvent is evaporated off to give 31.7 g of the expected product after crystallization from pentane. M.p.=92° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05726313 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-2ea15a5f5b1a44b1851d5776c77eecc6 |
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| 出典メモ | uspto-grants-1998_03 |
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