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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1643433Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1643433

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Benzyl-4-(pyridin-3-YL)piperidin-4-OLHCID 1094079—
EduktAmmonium formateHCID 2723923—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
LösungsmittelChloroformHCID 6212—
Produkt4-(Pyridin-3-yl)piperidin-4-olHCID 4989167—

Reaktionsbedingungen

Temperatur68 °C

Reaktionsschritte

(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%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08119805B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-e09f3ab50bd2422d8bb92ccb82c28e45
Quellennotizuspto-grants-2012_02