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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1609484생성일: 2026년 10월 24일

Acetic Acid → N-(1-azabicyclo[2.2.2]oct-3 yl)-N'-(3-chlorphenyl)-1,2-diaminoethane

https://huagongshe.com/ko/reaction/1609484

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1-Azabicyclo(2.2.2)octan-3-one, hydrochloride (1:1)HCID 102019—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물N1-(3-chlorophenyl)ethane-1,2-diamineHCID 11008376—
용매MethanolHCID 887—
생성물N-(1-azabicyclo[2.2.2]oct-3 yl)-N'-(3-chlorphenyl)-1,2-diaminoethaneHCID 1049297740.3%

반응 단계

To a stirred solution of N-(3-chlorophenyl)-1,2-diaminoethane (1 g; 0.00586 moles) in 25 ml of anhydrous methanol kept under nitrogen atmosphere, 3-quinuclidinone hydrochloride (1.01 g, 0.00627 moles) is added. The pH is adjusted to pH 6 by addition of glacial acetic acid. Sodium cyanoborohydride (0.74 g; 0.0117 moles) is added in two portions. The reaction mixture is refluxed for 10 hours, cooled and then filtered. After evaporation to dryness the residue is taken up with water, basified with 20% sodium hydroxide solution and extracted three times with ethyl acetate. The organic layer is washed with brine, dried over anhydrous sodium sulfate and, after filtration, evaporated to dryness. The residue is purified by silica gel flash-chromatography (methylene chloride-methanol30% ammonium hydroxide, 1.50:50:5 as eluant) to give the desired product as a clear oil (0.66 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05401750
출처 데이터셋uspto-grants-1995_03
ORD IDord-a64f5decd6194bda933578a1707e7a43
출처 메모uspto-grants-1995_03