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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507268Generated: October 27, 2026

Potassium Carbonate → 4-[4-Hydroxy-4-(4-methyl-benzyl)-piperidin-1-yl]-1-(4-methoxy-phenyl)-butan-1-one

https://huagongshe.com/reaction/507268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-4'-methoxybutyrophenoneHCID 96414—
Reactant4-(4-Methylbenzyl)-piperidin-4-olHCID 10536242—
SolventAcetonitrileHCID 6342—
Product4-[4-Hydroxy-4-(4-methyl-benzyl)-piperidin-1-yl]-1-(4-methoxy-phenyl)-butan-1-oneHCID 2312502777.6%

Reaction Conditions

Temperature107.5 °C

Reaction Steps

A mixture of 1.62 g of 4-chloro-1-(4-methoxy-phenyl)-butan-1-one (1), 1.20 g of 4-(4-methyl-benzyl)-piperidin-4-ol (2), 1.62 g of K2CO3, and 0.49 g of KI in acetonitrile (30 mL) was stirred and refluxed at 105 to 110° C. for 9 hours under nitrogen atmosphere. After the solvent was removed, ice water was added and the mixture was extracted with ethyl acetate. The organic layer was successively washed with water and brine and dried over MgSO4. After the solvent was removed, the obtained oily residue was purified by silica gel chromatography (chloroform:methanol=20/1 to 10/1) and the purified product was recrystallized from AcOEt/Et2O to afford 1.73 g of compound (3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786140B2
Source datasetuspto-grants-2010_08
ORD IDord-bedd0e60b188490b9c21bc181597928e
Source noteuspto-grants-2010_08