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HRID 6791作成日:2026年10月23日

Propargyl bromide → 4-Methyl-1-(prop-2-yn-1-yl)piperidine

https://huagongshe.com/ja/reaction/6791

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl bromideHCID 7842—
反応物Potassium CarbonateHCID 11430—
反応物4-MethylpiperidineHCID 69381—
溶媒AcetoneHCID 180—
生成物4-Methyl-1-(prop-2-yn-1-yl)piperidineHCID 1135550992%

反応条件

温度50 °C

反応手順

At 0–5° C., propargyl bromide (12.01 g) was added dropwise with stirring to a suspension of 4-methylpiperidine (10.0 g) and potassium carbonate (13.96 g) in dry acetone (80 ml). The mixture was stirred at 50° C. for 6 hours and then filtered. The filtrate was concentrated under reduced pressure and the residue was taken up in dichloromethane. The organic phase was washed with water (3×15 ml), dried with sodium sulfate and concentrated under reduced pressure. Distillation of the residue under reduced pressure gave 12.73 g of an oil of boiling point 60° C./16 mm Hg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084158B2
出典データセットuspto-grants-2006_08
ORD IDord-3d1eef909b754b8da0b694cdccfec3a6
出典メモuspto-grants-2006_08