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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1533901생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1533901

반응식

참여 물질

역할이름HCID투입량
반응물N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamideHCID 960610—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물N-[4-(1-Piperazinyl)phenyl]acetamideHCID 1563176156.5%

반응 단계

This compound was prepared by the hydrogenation of 7.7 g (0.025 mol) 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%) of crude product. A 0.5 g portion was recrystallized from methanol/petroleum ether to give a cream colored solid, mp 191°-193° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05086055
출처 데이터셋uspto-grants-1992_02
ORD IDord-8caf3478076c484ba7009e19d11347c5
출처 메모uspto-grants-1992_02