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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689902Generated: October 31, 2026

Water → Ethyl 1-benzylpiperidine-4-carboxylate

https://huagongshe.com/reaction/1689902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
SolventAcetonitrileHCID 6342—
ProductEthyl 1-benzylpiperidine-4-carboxylateHCID 90423—

Reaction Conditions

Temperature78 °C

Reaction Steps

Amine preparation: To a solution of piperidine-4-carboxylic acid ethyl ester (3.0 g) stirring in dry MeCN (30 mL) was added potassium carbonate (2.90 g) followed by benzyl bromide (2.5 mL). The mixture was warmed to 78° C. After 3 h the mixture was cooled, poured into water (100 mL) and extracted into ethyl acetate, dried (MgSO4) and the solvent removed in vacuo. The residue was purified using flash chromatography to give 1-benzyl-piperidine-4-carboxylic acid ethyl ester (2.17 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153629B2
Source datasetuspto-grants-2012_04
ORD IDord-9f23ba576b7148b08327354b408a7608
Source noteuspto-grants-2012_04