Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196490Generated: November 1, 2026

1-(4-[(Allyloxy)carbonyl]phenyl)piperidine-4-carboxylic acid ethyl ester → 4-[4-(Ethoxycarbonyl)piperidin-1-YL]benzoic acid

https://huagongshe.com/reaction/2196490

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-[(Allyloxy)carbonyl]phenyl)piperidine-4-carboxylic acid ethyl esterHCID 57986702—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
SolventMorpholineHCID 8083—
Product4-[4-(Ethoxycarbonyl)piperidin-1-YL]benzoic acidHCID 1906386465.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4.74 g of 1-{4-[(allyloxy)carbonyl]phenyl}piperidine-4-carboxylic acid ethyl ester in 75 ml of THF, 2.10 ml of morpholine and 390 mg of tetrakis(triphenylphosphine)palladium were added, and the mixture was stirred at 60° C. for 1.5 hours. After the solvent was evaporated under reduced pressure, EtOAc was added to the residue, and the reaction solution was washed with NaHCO3 aq. three times. To the collected saturated NaHCO3 aq., conc. HCl was added, and the produced precipitate was collected by filtration and dried under reduced pressure to obtain 2.73 g of 4-[4-(Ethoxycarbonyl)piperidin-1-yl]benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338429B2
Source datasetuspto-grants-2012_12
ORD IDord-272c776520d84a2397fe7eee6d517a18
Source noteuspto-grants-2012_12