Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981615Generated: October 25, 2026

Water → 3-(1-((Benzyloxy)carbonyl)piperidin-4-yl)propanoic acid

https://huagongshe.com/reaction/981615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzyl 4-(3-ethoxy-3-oxopropyl)piperidine-1-carboxylateHCID 14989191—
SolventEthanolHCID 702—
Product3-(1-((Benzyloxy)carbonyl)piperidin-4-yl)propanoic acidHCID 9895315100%

Reaction Steps

To a stirred and cooled (15° C.) mixture of 11.1 parts of potassium hydroxide and 96 parts of water was added dropwise a solution of 31.8 parts of ethyl 1-[(phenylmethoxy)carbonyl]-4-piperidinepropanoate in 38 parts of ethanol during 20 minutes. Upon complete addition, stirring was continued overnight at room temperature. The reaction mixture was evaporated at <50° C. The reaction mixture was poured into crushed ice and treated with concentrated hydrochloric acid. The separated aqueous layer was extracted with dichloromethane. The extract was dried, filtered and evaporated, yielding 29 parts (100%) of 1-[(phenylmethoxy)carbonyl]-4-piperidinepropanoic acid as a residue (int. 33).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04992433
Source datasetuspto-grants-1991_02
ORD IDord-b7f53fc2571149ce864bd56a2db2390b
Source noteuspto-grants-1991_02