돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 743852생성일: 2026년 10월 25일

4-Benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzene → 4-[4-(4-Pyridyl)piperazin-2-one-1-yl]phenol

https://huagongshe.com/reaction/743852

반응식

참여 물질

역할이름HCID투입량
반응물4-Benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzeneHCID 54227295—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물4-[4-(4-Pyridyl)piperazin-2-one-1-yl]phenolHCID 18918415—

반응 단계

To a solution of the product of step (i) (1.1 g) in a mixture of methanol (500 ml) and tetrahydrofuran (100 ml) was added 30% palladium-on-charcoal catalyst (300 mg) and the mixture stirred in an atmosphere of hydrogen at ambient temperature and pressure until all the starting material had been consumed. After removal of the catalyst by filtration, the solvent was evaporated in vacuo to give 4-[4-(4-pyridyl)piperazin-2-one-1-yl]phenol as a colourless solid, essentially one spot by tlc, which was used without further purification or characterisation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05556977
출처 데이터셋uspto-grants-1996_09
ORD IDord-1e2ddc42f7424b8fbe1cba4ab884d3a6
출처 메모uspto-grants-1996_09