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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187859Generated: November 2, 2026

1-Chloro-4-(chloromethyl)benzene → 3-Amino-1-(4-chlorobenzyl)homopiperidine

https://huagongshe.com/reaction/2187859

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantPotassium CarbonateHCID 11430—
ReactantAzepan-3-amineHCID 2756445—
SolventAcetonitrileHCID 6342—
Product3-Amino-1-(4-chlorobenzyl)homopiperidineHCID 1842623993%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 3-aminohomopiperidine (1.71 g, 15 mmol) in CH3CN (45 mL) was treated with p-chlorobenzyl chloride (463 mg, 2.9 mmol) and K2CO3 (828 g, 6 mmol) and heated to 70° C. for 9 h. The reaction mixture was cooled to 25° C. and concentrated to afford a yellow solid. The residue was partitioned between H2O (5 mL) and EtOAc (50 mL), and extracted with EtOAc (2×50 mL). The combined organic extracts were washed with brine (20 mL), dried (Na2SO4) and concentrated. The resulting yellow oil was purified by chromatography (SiO2, 5-20% CH3OH—CH2Cl2 gradient elution) to afford the desired product as a yellow oil (639 mg, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410566B1
Source datasetuspto-grants-2002_06
ORD IDord-5b6991659ceb44f0b2f262adf4c84234
Source noteuspto-grants-2002_06