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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030896Generated: November 2, 2026

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

https://huagongshe.com/reaction/1030896

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 numberUS05106973
Source datasetuspto-grants-1992_04
ORD IDord-c813736bd6e74d8fb358b0f1a9274a36
Source noteuspto-grants-1992_04