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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223706Generated: October 31, 2026

Iodine → 1-Benzyl-4-(4-methylphenyl)piperidin-4-ol

https://huagongshe.com/reaction/2223706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-BromotolueneHCID 7805—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantAmmonium ChlorideHCID 25517—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product1-Benzyl-4-(4-methylphenyl)piperidin-4-olHCID 198608—

Reaction Steps

A solution of 4-bromotoluene (1.017 g, 5.94 mmol) in anhydrous Et2O (6 mL), is added dropwise to a mixture of Mg (0.159 g, 6.54 mmol) and a catalytic amount of I2 (0.015 g, 0.26 mmol) in anhydrous Et2O (10 mL). The mixture is stirred at reflux for 5 h under nitrogen. To this cloudy solution is added dropwise at 0° C., a solution of N-benzyl-4-piperidone (1.063 mL, 5.94 mmol) in anhydrous Et2O (6 mL) and the mixture is stirred at reflux for 1.5 h. After cooling, the mixture is poured into sat. NH4Cl (20 mL) and extracted with EtOAc (3×30 mL). The combined organic extracts are washed with brine, dried (MgSO4), filtered and concentrated to provide a crude oil. Flash chromatography (EtOAc/Hex: 3/7) affords the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375227B2
Source datasetuspto-grants-2008_05
ORD IDord-bd1f8038259b4d7cb355e48acc13a189
Source noteuspto-grants-2008_05