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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6792생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물PiperidineHCID 8082—
반응물PhenylacetyleneHCID 10821—
촉매Cuprous chlorideHCID 62652—
용매1,4-DioxaneHCID 31275—
생성물1-(3-Phenyl-2-propyn-1-yl)piperidineHCID 20071165.3%

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084158B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-a76fbde539d14fbe965fa11a289cc844
출처 메모uspto-grants-2006_08