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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1643433생성일: 2026년 10월 26일

1-Benzyl-4-(pyridin-3-YL)piperidin-4-OL → 4-(Pyridin-3-yl)piperidin-4-ol

https://huagongshe.com/reaction/1643433

반응식

참여 물질

역할이름HCID투입량
반응물1-Benzyl-4-(pyridin-3-YL)piperidin-4-OLHCID 1094079—
반응물Ammonium formateHCID 2723923—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
생성물4-(Pyridin-3-yl)piperidin-4-olHCID 4989167—

반응 조건

온도68 °C

반응 단계

(Apparatus: 1 I three-necked flask with condenser) Palladium on charcoal (10%, catalytic amount) was added to a solution of 1-benzyl-4-(pyridin-3-yl)piperidin-4-ol (32 g) in methanol (220 ml), followed by ammonium formate solution (22.7 g in 50 ml of water). The reaction mixture was refluxed at 68° C. overnight. Thin layer chromatography control: 20% methanol in chloroform. The mixture was filtered over Celite and the filtrate was concentrated in vacuo. The residue was washed with acetone (100 ml) in order to obtain the desired compound in a pure form. Yield: 17.3 g (81%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08119805B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-e09f3ab50bd2422d8bb92ccb82c28e45
출처 메모uspto-grants-2012_02