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HRID 1839作成日:2026年10月24日

Diethyl Ether → 1,4-Dibenzyl-4-cyanopiperidine

https://huagongshe.com/ja/reaction/1839

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Benzyl BromideHCID 7498—
反応物TetrahydrofuranHCID 8028—
反応物4-CyanopiperidineHCID 138223—
反応物Lithium diisopropylamideHCID 2724682—
溶媒CyclohexaneHCID 8078—
生成物1,4-Dibenzyl-4-cyanopiperidineHCID 22741742—

反応条件

温度-50 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726313
出典データセットuspto-grants-1998_03
ORD IDord-2ea15a5f5b1a44b1851d5776c77eecc6
出典メモuspto-grants-1998_03