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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248873생성일: 2026년 10월 26일

Piperidine → 2-(N-Benzyl-N-methylamino)-1-(N-piperidinyl)ethane

https://huagongshe.com/reaction/248873

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물Sodium BicarbonateHCID 516892—
반응물N-(2-Chloroethyl)-N-methylbenzylamine hydrochlorideHCID 12822620—
용매EthanolHCID 702—
생성물2-(N-Benzyl-N-methylamino)-1-(N-piperidinyl)ethaneHCID 2320843658.5%

반응 단계

A solution of piperdine (1.16 g, 13.6 mmol), the title compound of Step 10 (3.0 g, 13.6 mmol) and NaHCO3 (3.94 g, 46.9 mmol) in EtOH (24 mL) was refluxed overnight in a modification of the procedure of Bach, et al. [J. Am. Chem. Soc. 79, 2221-2225 (1957)]. After filtration, the filtrate was concentrated to a yellow murky oil. The oil was dissolved into a 1.0M KOH solution (10 mL) and was extracted with EtOAc (3×5 mL). The organic layer was washed with a 5% NaHCO3, solution (5 mL), H2O (5 mL), and brine (5 mL) and then was dried over MgSO4. The filtrate was concentrated and purified by medium pressure column chromatography on silica gel [eluting NH4OH-EtOH-CHCl3 (1:5:94)] to give 1.85 g (58% yield) of the title compound as an oil. The proton spectral data were consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05212185
출처 데이터셋uspto-grants-1993_05
ORD IDord-a4cf1aa789c24709be68a72691319433
출처 메모uspto-grants-1993_05