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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484483Generated: October 26, 2026

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

https://huagongshe.com/reaction/484483

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 wa 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 numberUS05231184
Source datasetuspto-grants-1993_07
ORD IDord-073f2d46a8ad45f1ad135a37e48d8563
Source noteuspto-grants-1993_07