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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1675086생성일: 2026년 10월 25일

Benzyl 4-hydroxy-4-(pyridin-3-yl)piperidine-1-carboxylate → 4-(Pyridin-3-yl)piperidin-4-ol

https://huagongshe.com/reaction/1675086

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl 4-hydroxy-4-(pyridin-3-yl)piperidine-1-carboxylateHCID 21480587—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물4-(Pyridin-3-yl)piperidin-4-olHCID 498916780%

반응 단계

Benzyl 4-hydroxy-4-(pyridin-3-yl)piperidine-1-carboxylate (32.7 g, 104.69 mmol) was dissolved in ethanol (350 mL) and hydrogenated over 10% palladium on carbon (3.2 g) at 2 bar pressure at 30° C. After hydrogen uptake was complete, the mixture was filtered through a pad of diatomaceous earth to remove the catalyst and the pad was washed with ethanol. The filtrate was concentrated to dryness under vacuum to give an oil which crystallised on standing overnight. The solid was triturated with MTBE (100 mL), collected by filtration, washed with MTBE (2×50 ml) and dried in a vacuum oven at 40° C. to afford 4-(pyridin-3-yl)piperidin-4-ol (14.9 g, 80%) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08003649B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-dae26efd5249466eb1c34c55007141d4
출처 메모uspto-grants-2011_08