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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1156028생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1156028

반응식

참여 물질

역할이름HCID투입량
반응물Piperidine, 1-methyl-4-(4-nitrophenoxy)-4-phenyl-HCID 3060390—
촉매PlatinumHCID 23939—
용매EthanolHCID 702—
생성물Piperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl-HCID 306039274.4%

반응 단계

51 g of 1-methyl-4-(4-nitrophenoxy)-4-phenylpiperidine are dissolved in 1.5 liters of ethanol and are hydrogenated under a hydrogen pressure of 1 atmosphere in the presence of platinum. The catalyst is filtered off, the filtrate is concentrated to 300 ml and crystals (which have separated out) are collected. 34.3 g of the title compound of m.p. 173° to 174° C. are obtained by successive concentration of the filtrate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04333942
출처 데이터셋uspto-grants-1982_06
ORD IDord-8ad115a3f6d441419d4866e6503e5fc5
출처 메모uspto-grants-1982_06