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HRID 228500Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/228500

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 NH3 MeOH 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
PatentnummerUS07560463B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-777cd9e8c37d4ae192acd6077e7596a1
Quellennotizuspto-grants-2009_07