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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28142생성일: 2026년 10월 25일

Allyl bromide → N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine

https://huagongshe.com/reaction/28142

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물TriethylamineHCID 8471—
반응물N-(4-chlorophenyl)piperidin-4-amineHCID 7183033—
용매BenzeneHCID 241—
생성물N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamineHCID 23339007—

반응 단계

To a stirred mixture of 15 parts of N-(4-chlorophenyl)-4-piperidinamine, 12 parts of N,N-diethylethanamine in 130 parts of benzene is added dropwise a solution of 10.3 parts of 3-bromo-1-propene in 70 parts of benzene. Upon completion, the whole is stirred first for 20 h. 30 at room temperature and further for 40 minutes at reflux. The reaction mixture is cooled, filtered and the filtrate is evaporated. The residue is taken up in 1,1'-oxybisethane and treated with activated charcoal. The latter is filtered off and the 1,1'-oxybisethane is evaporated again, yielding 2.9 parts of N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine; mp. 90° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04225606
출처 데이터셋uspto-grants-1980_09
ORD IDord-892bec6fc0e0497e96b6d153d36e6999
출처 메모uspto-grants-1980_09