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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323698생성일: 2026년 10월 24일

N,N-Dimethylaniline → 4-((10,11-dihydro-5H-dibenz[b,f]azepin-5-yl)carbonyl)-1-benzylpiperidine

https://huagongshe.com/ko/reaction/323698

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물IminodibenylHCID 10308—
반응물1-Benzyl-4-piperidinecarbonylchloride hydrochlorideHCID 19261354—
용매TolueneHCID 1140—
생성물4-((10,11-dihydro-5H-dibenz[b,f]azepin-5-yl)carbonyl)-1-benzylpiperidineHCID 1926135536.4%

반응 단계

A mixture of 1-benzyl-4-piperidinecarbonylchloride hydrochloride (25.0 g, 91 mmol), 10,11-dihydro-5H-dibenzo[b,f]azepine (17.6 g, 90 mmol), N,N-dimethylaniline (25 ml) and toluene (150 ml) was heated at reflux temperature under stirring for 14 h. The mixture was decanted and to the remaining solid 10% ammonia (100 ml) and chloroform (150 ml) were added. The phases were separated and the combined toluene and chloroform phases were dried (K2CO3) and evaporated in vacuo. The residue was purified by chromatography on silica gel (300 g) using benzene and ethyl acetate as eluents. The crude base was crystallised from cyclohexane, yielding 13.0 g (36%) of 4-((10,11-dihydro-5H-dibenz[b,f]azepin-5-yl)carbonyl)-1-benzylpiperidine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06214816B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-88a4d356da2349a5b1d876b9ed2e1347
출처 메모uspto-grants-2001_04