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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066983Generated: November 2, 2026

Benzoyl chloride → N-(1-(Phenylmethyl)-4-piperidinyl)benzamide

https://huagongshe.com/reaction/1066983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(1-(Phenylmethyl)-4-piperidinyl)benzamideHCID 4059887.7%

Reaction Steps

To a biphasic solution of 4-amino-1-benzylpiperidine (6.0 g, 31.6 mmol), K2CO3 (8.71 g, 63.1 mmol) in CH2Cl2 (200 mL) and water (100 mL) was added benzoyl chloride (4.86 g, 34.7 mmol) in 20 mL of CH2Cl2 at 0° C. with stirring. After stirring for 4 h at room temperature, the layers were separated. The organic layer was washed with water, dried over MgSO4 and filtered. The solvent was removed in vacuo to obtain 1-benzyl-4-benzamidopiperidine (8.16 g, 87% yield) as a white solid. It was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245773B1
Source datasetuspto-grants-2001_06
ORD IDord-7aa16512fe6d405aa32028c1a7a3ebf4
Source noteuspto-grants-2001_06