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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277159Generated: October 25, 2026

2-Phenylpropionic acid → 1-(4-Hydroxypiperidin-1-yl)-3-phenylpropan-1-one

https://huagongshe.com/reaction/277159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Phenylpropionic acidHCID 10296—
ReactantSodium HydroxideHCID 14798—
ReactantBenzenepropanoyl chlorideHCID 64801—
ReactantPiperidin-4-olHCID 79341—
SolventTolueneHCID 1140—
Product1-(4-Hydroxypiperidin-1-yl)-3-phenylpropan-1-oneHCID 2217516239%

Reaction Steps

This amine was synthesized in accordance with the method of Scheme 37. To 4 g (40 mmol) of 4-hydroxypiperidine in 20 mL of toluene was added phenylpropionyl chloride (derived from 6 g (40 mmol) of phenylpropionic acid in excess thionyl chloride). To the mixture was added excess 2N aqueous NaOH. After stirring 24 hours, the toluene layer was discarded and the aqueous phase was extracted with CH2Cl2, dried, and evaporated under vacuum to give 3.63 g (39%) of 1-(3-phenylpropionyl)-4-hydroxypiperidine (134). GC/MS indicated 100% purity with a molecular ion of 233.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355660B1
Source datasetuspto-grants-2002_03
ORD IDord-20902f74a8974b1e835cf06a9590e6d8
Source noteuspto-grants-2002_03