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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966418Generated: October 30, 2026

Benzyl Bromide → Ethyl 1-benzylpiperidine-4-carboxylate

https://huagongshe.com/reaction/966418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-benzylpiperidine-4-carboxylateHCID 9042374.2%

Reaction Steps

30 g of benzyl bromide are added dropwise to a mixture of 25 g of ethyl isonipecotate and 25 g of K2CO3 in 125 ml of DMF, while maintaining the temperature of the reaction mixture between 25 and 30° C., and the resulting mixture is then stirred at RT for 1 hour. The reaction mixture is poured onto 1 liter of ice-cold water and extracted twice with ether, the organic phase is washed with water and dried over MgSO4, and the solvent is evaporated off under vacuum. The resulting oil obtained is distilled off under reduced pressure. 29.2 g of the expected product are obtained; b.p.=120-122° C. at 2.7 Pa.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951940B2
Source datasetuspto-grants-2005_10
ORD IDord-9a71b7f294e24d63b42ba84c7ca1bd3f
Source noteuspto-grants-2005_10