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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26756생성일: 2026년 10월 25일

Allyl bromide → N-(4-chlorophenyl)-N-[1-(2-propenyl)-4-piperidinyl]benzeneacetamide hydrochloride

https://huagongshe.com/reaction/26756

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물TriethylamineHCID 8471—
반응물N-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamideHCID 162188—
용매BenzeneHCID 241—
생성물N-(4-chlorophenyl)-N-[1-(2-propenyl)-4-piperidinyl]benzeneacetamide hydrochlorideHCID 23339063—

반응 단계

To a stirred solution of 5 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide, 3.8 parts of N,N-diethylethanamine in 200 parts of benzene are added portionwise 5 parts of 3-bromo-1-propene. After the addition is complete, the whole is heated for 21 hours at a temperature between 50°-60° C. The reaction mixture is cooled and filtered. The filtrate is washed successively with water, sodium hydrogen carbonate solution and water, dried over potassium carbonate and evaporated. The oily residue is converted into the hydrochloride salt in 1,1'-oxybisethane and 2-propanone, yielding 4 parts of N-(4-chlorophenyl)-N-[1-(2-propenyl)-4-piperidinyl]benzeneacetamide hydrochloride; mp. 225.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04151286
출처 데이터셋uspto-grants-1979_04
ORD IDord-cbff7e24092742ffa2a9ec10e70cf115
출처 메모uspto-grants-1979_04