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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131042Generated: November 1, 2026

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

https://huagongshe.com/reaction/131042

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 numberUS07381719B2
Source datasetuspto-grants-2008_06
ORD IDord-cc3bf634e4934291b989af2331df8d41
Source noteuspto-grants-2008_06