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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842328Generated: November 2, 2026

Water → Ethyl 1-benzylpiperidine-4-carboxylate

https://huagongshe.com/reaction/1842328

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 numberUS08946217B2
Source datasetuspto-grants-2015_02
ORD IDord-e3ed691625e6423bb45f2bd4d980a142
Source noteuspto-grants-2015_02