Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131049Generated: October 25, 2026

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

https://huagongshe.com/reaction/131049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-butan-1-oneHCID 59730198—
SolventDiethylene GlycolHCID 8117—
Product3-Butyl-1-(4-methoxy-benzyl)-piperidineHCID 5973040189%

Reaction Conditions

Temperature120 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381719B2
Source datasetuspto-grants-2008_06
ORD IDord-6e0803076ca548148366ebe5a232277d
Source noteuspto-grants-2008_06