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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1087815생성일: 2026년 10월 27일

N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamide → N-[4-(1-Piperazinyl)phenyl]acetamide

https://huagongshe.com/reaction/1087815

반응식

참여 물질

역할이름HCID투입량
반응물N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamideHCID 960610—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물N-[4-(1-Piperazinyl)phenyl]acetamideHCID 1563176156%

반응 단계

This compound was prepared by the hydrogenation of 7.7 (0.025 mole) of N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]acetamide in 100 ml of methanol using palladium on carbon as the catalyst. The solution was filtered and the filtrate concentrated under reduced pressure to give an oil which crystallized. The solid was dissolved in a minimum amount of a methylene chloride/10% methanol solution and passed through a 100 g Florisil® column. The desired fractions were concentrated to an oil under reduced pressure which crystallized to give 3.1 g (56%) crude product. A 0.5 g portion was recrystallized from methanol/petroleum ether to give cream colored solid, m.p. 191°-193° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04960776
출처 데이터셋uspto-grants-1990_10
ORD IDord-fea3129dcd2645d18642fb590b795be2
출처 메모uspto-grants-1990_10