Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280989Generated: October 25, 2026

1-Chloro-4-(chloromethyl)benzene → 3-Carbamoyl-1-(4-chlorobenzyl)piperidine

https://huagongshe.com/reaction/1280989

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantTriethylamineHCID 8471—
Reactant3-PiperidinecarboxamideHCID 92980—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-Carbamoyl-1-(4-chlorobenzyl)piperidineHCID 284579755.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of nipecotamide (6.40 g, 50 mmol) in CH3CN (150 mL) and ethanol (20 mL) was treated with Et3N (7.0 mL, 50 mmol) and 4-chlorobenzyl chloride (8.05 g, 50 mmol). The reaction mixture was stirred at 50° C. for 16 h. After cooling to room temperature, saturated aqueous NaHCO3 (50 mL) and water (150 mL) was added to the reaction mixture. The mixture was extracted with ethyl acetate (150 mL×3) and the combined organic layers were washed with brine, dried (Na2SO4) and concentrated to give a pale red solid. The crude solid was washed with ether (100 mL) to afford 3-carbamoyl-1-(4-chlorobenzyl)piperidine (6.98 g, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451842B1
Source datasetuspto-grants-2002_09
ORD IDord-8f36a84adc9b485faf9c12452aabe87d
Source noteuspto-grants-2002_09