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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1079392생성일: 2026년 10월 26일

Piperidine → Piperidine, 1-(4-nitrophenyl)-

https://huagongshe.com/reaction/1079392

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물p-FluoronitrobenzeneHCID 9590—
용매DimethylformamideHCID 6228—
생성물Piperidine, 1-(4-nitrophenyl)-HCID 81049—

반응 단계

A solution of p-fluoronitrobenzene (31.8 ml) in dimethylformamide (200 ml) was ice-cooled and to this was added piperidine (60 ml) dropwise, followed by stirring with ice cooling for 2 hours. After the solvent was distilled off, the residual oily product was dissolved in ethyl acetate ester (200 ml), followed by washing in turn with aqueous saturated solution of sodium bicarbonate and water. Then, the solution was dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was recrystallized from n-hexane to obtain N-(4-nitrophenyl)piperidine as yellow crystals (52.8 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05580883
출처 데이터셋uspto-grants-1996_12
ORD IDord-2cf7a327371f4730a5c5bfa29490dc36
출처 메모uspto-grants-1996_12