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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1154728생성일: 2026년 10월 25일

Methanol → Benzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)-

https://huagongshe.com/reaction/1154728

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물1-(4-Methoxyphenyl)-4-(4-nitrophenyl)piperazineHCID 5134657—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물Benzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)-HCID 15440674%

반응 단계

A mixture of 12 parts of 1-(4-methoxyphenyl)-4-(4-nitrophenyl)piperazine, 200 parts of methanol and 225 parts of tetrahydrofuran is hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and washed with N,N-dimethylacetamide. The filtrate is poured onto water. The precipitated product is filtered off and crystallized from 1-butanol, yielding 8 parts (74%) of 4-[4-(4-methoxyphenyl)-1-piperazinyl]benzenamine; mp. 191.8° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04490530
출처 데이터셋uspto-grants-1984_12
ORD IDord-25c3423e6e894d7bb0b00ccbd2a57ac2
출처 메모uspto-grants-1984_12