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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323696생성일: 2026년 10월 24일

N,N-Dimethylaniline → 3-(10,11-dihydro-5H-dibenz[b,f]azepin-5-ylcarbonyl)-1-benzylpiperidine hydrogen oxalate hemihydrate

https://huagongshe.com/ko/reaction/323696

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물Oxalic AcidHCID 971—
반응물IminodibenylHCID 10308—
반응물1-Benzyl-3-piperidinecarbonyl chloride hydrochlorideHCID 22006204—
용매AcetoneHCID 180—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물3-(10,11-dihydro-5H-dibenz[b,f]azepin-5-ylcarbonyl)-1-benzylpiperidine hydrogen oxalate hemihydrateHCID 13172249039%

반응 단계

A mixture of 1-benzyl-3-piperidinecarbonyl chloride hydrochloride (12.5 g, 45.6 mmol), 10,11-dihydro-5H-dibenz[b,f]azepine (8.9 g, 45.6 mmol), N,N-dimethylaniline (15 ml) and toluene (100 ml) was heated at reflux temperature for 14 h. The mixture was decanted and to the remaining solid 10% ammonia (100 ml) and chloroform (100 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 gradient chromatography on silica gel (200 g) using benzene and chloroform as eluents. The chloroform fractions afforded the crude product. This was dissolved in ethanol (30 ml) and neutralised with oxalic acid in acetone, affording 8.8 g (39%) of 3-(10,11-dihydro-5H-dibenz[b,f]azepin-5-ylcarbonyl)-1-benzylpiperidine hydrogen oxalate hemihydrate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06214816B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-23e0c2ad46d14ebd92bb5f3115dccfc6
출처 메모uspto-grants-2001_04