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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2285916생성일: 2026년 10월 27일

Piperidine, 1-methyl-4-(4-nitrophenoxy)-4-phenyl- → Piperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl-

https://huagongshe.com/reaction/2285916

반응식

참여 물질

역할이름HCID투입량
반응물Piperidine, 1-methyl-4-(4-nitrophenoxy)-4-phenyl-HCID 3060390—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물Piperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl-HCID 306039250.3%

반응 단계

A solution of 1-methyl-4-(4-nitrophenoxy)-4-phenylpiperidine (4.4 g, 14.1 mM) in methanol (250 ml) was hydrogenated at 1 atmosphere and ambient temperature over 5% palladium on charcoal (500 mg) until the theoretical uptake of hydrogen had occurred (about 2 hours). The catalyst was removed by filtration and the solvent evaporated under reduced pressure. Recrystallisation of the residue from IPA gave the title compound (2 g) m.p. 174°-5°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04325953
출처 데이터셋uspto-grants-1982_04
ORD IDord-087ae6c0a6d144b4b3419ed8322470da
출처 메모uspto-grants-1982_04