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HRID 131049Erstellt: 24. Oktober 2026

Potassium Hydroxide → 3-Butyl-1-(4-methoxy-benzyl)-piperidine

https://huagongshe.com/de/reaction/131049

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktHydrazine hydrate (1:1)HCID 24654—
EduktAmmonium ChlorideHCID 25517—
Edukt1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-butan-1-oneHCID 59730198—
LösungsmittelDiethylene GlycolHCID 8117—
Produkt3-Butyl-1-(4-methoxy-benzyl)-piperidineHCID 5973040189%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Combine 1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-butan-1-one (356.0 mg, 0.95 mmol), Diethylene glycol (15 mL), KOH (479.0 mg, 8.54 mmol), and Hydrazine-monohydrate (1.8 mL) at room temperature under a Nitrogen atmosphere. Heat the reaction mixture to 120° C. for 2 hours and then 220° C. for 24 hours. Cool reaction to room temperature and then pour the reaction mixture over sat NH4Cl (aq). Extract with Ethyl acetate, wash with brine, and dry over Na2SO4. Concentrate under reduced pressure and flash chromatograph using 3% 1N NH3MeOH in CH2Cl2 to give 220.7 mg (89% yield) of the title compound: 1H NMR (500 MHz, CDCl3); 0.7-0.9 (3H, m), 1.1-1.4 (4H, m), 1.5-1.7 (4H, m), 1.7 (1H, d), 1.9 (1H, t), 2.8 (2H, t), 3.4 (2H, dd), 3.6-3.7 (3H, m), 3.8 (3H, s), 6.8 (2H, d), 7.2 (2H, d); MS m/z 262 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381719B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-6e0803076ca548148366ebe5a232277d
Quellennotizuspto-grants-2008_06