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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8382생성일: 2026년 10월 23일

Piperidine → 4-Piperidinylbut-1-ene

https://huagongshe.com/ko/reaction/8382

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물Homoallyl bromideHCID 21241—
생성물4-Piperidinylbut-1-eneHCID 456228293.4%

반응 단계

A mixture of 1-bromo-3-butene (1.35 g, 10 mmol) and piperidine (1.70 g, 20 mmol) neat was refluxed under nitrogen atmosphere for 3 h. Cooled to RT, filtered and dissolved into ethyl ether (40 mL). Then solution was washed with water (2×30 mL) and dried over anhydrous Na2SO4, filtered and evaporated to dryness to yield 1.3 g (74.15%) oily 1-piperidyl-3-butene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087757B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-2927bd8c3c9846bbb36c39855a81a50c
출처 메모uspto-grants-2006_08