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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380486Generated: October 30, 2026

(3-Bromopropyl)benzene → 1-Benzyl-4-(3-phenylpropyl)piperidin-4-ol

https://huagongshe.com/reaction/380486

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Bromopropyl)benzeneHCID 12503—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
Product1-Benzyl-4-(3-phenylpropyl)piperidin-4-olHCID 2262447877.3%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of 3.8 mL (25 mmol) of 1-bromo-3-phenyl propane in 200 mL of ether at −78° C. was slowly added 30 mL (50 mmol) of t-BuLi (1.7 M in pentane). The reaction mixture was warmed to −20° C. for 15 min, then it was recooled to −78° C. To this reaction mixture was slowly added a solution of 2.61 g (13.8 mmol) of 1-benzyl-4-piperidone in 20 mL of ether. After 15 min, the reaction mixture was poured into, 200 mL of sat'd NH4Cl solution. The reaction mixture was extracted with ethyl acetate and the combined organic fractions were washed with sat'd NaCl solution, dried over MgSO4 filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes: ethyl acetate, 1:1) to give 3.3 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303593B1
Source datasetuspto-grants-2001_10
ORD IDord-cf6892b86a5141ed959c210795866f75
Source noteuspto-grants-2001_10