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HRID 11228作成日:2026年10月24日

Cyanide → 1,1'-Bipiperidine

https://huagongshe.com/ja/reaction/11228

反応式

関与物質

役割名称HCID仕込み量
反応物CyanideHCID 5975—
反応物TetrahydrofuranHCID 8028—
反応物HCID 178418689HCID 178418689—
溶媒Diethyl EtherHCID 3283—
生成物1,1'-BipiperidineHCID 6827979%

反応条件

温度25 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098213B2
出典データセットuspto-grants-2006_08
ORD IDord-70419371049d4118a56e44f216f0f529
出典メモuspto-grants-2006_08