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HRID 6792作成日:2026年10月23日

Hydrochloric Acid → 1-(3-Phenyl-2-propyn-1-yl)piperidine

https://huagongshe.com/ja/reaction/6792

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物FormaldehydeHCID 712—
反応物PiperidineHCID 8082—
反応物PhenylacetyleneHCID 10821—
触媒Cuprous chlorideHCID 62652—
溶媒1,4-DioxaneHCID 31275—
生成物1-(3-Phenyl-2-propyn-1-yl)piperidineHCID 20071165.3%

反応条件

温度25 °C

反応手順

With stirring, a solution of phenylacetylene (10.2 g) in dioxane (10 ml), a solution of piperidine (13.3 g) in dioxane (10 ml) and copper(I) chloride (0.1 g) were added successively to a suspension of paraformaldehyde (3.6 g) in dioxane (10 ml). The mixture was heated under reflux for 6 hours, allowed to cool to 25° C. and acidified using 20% strength hydrochloric acid. The solution was washed with diethyl ether and the aqueous phase was made alkaline using 50% strength aqueous sodium hydroxide solution and extracted with diethyl ether (3×100 ml). The organic phase was dried with magnesium sulfate and concentrated completely. Distillation of the residue under reduced pressure gave an oil (13.0 g) of boiling point 95° C./0.045 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-a76fbde539d14fbe965fa11a289cc844
出典メモuspto-grants-2006_08