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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492647Generated: October 30, 2026

Potassium Hydroxide → 1-(4-Methoxy-benzyl)-3-propyl-piperidine

https://huagongshe.com/reaction/492647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-propan-1-oneHCID 59730345—
SolventDiethylene GlycolHCID 8117—
Product1-(4-Methoxy-benzyl)-3-propyl-piperidineHCID 5973004740%

Reaction Conditions

Temperature120 °C

Reaction Steps

Combine 1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-propan-1-one (277.3 mg, 1.07 mmol), Diethylene glycol (10 mL), KOH (178.0 mg, 3.18 mmol), and Hydrazine-monohydrate (1.0 mL) at room temperature under a Nitrogen atmosphere. Heat the reaction mixture to 120° C. for 2 hours and then 220° C. for 4 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 105.2 mg (40% yield) of the title compound: 1H NMR (500 MHz, CDCl3); 0.9 (3H, t), 1.1-1.4 (4H, m), 1.5-1.7 (3H, m), 1.7 (1H, d), 1.9 (1H, td), 2.7-2.9 (2H, m), 3.5 (2H, dd), 3.8 (3H, s), 6.8 (2H, d), 7.2 (2H, d); MS m/z 248 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531557B2
Source datasetuspto-grants-2009_05
ORD IDord-d777ed9e91214ac6bc46a320cab7d7fa
Source noteuspto-grants-2009_05