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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972890Generated: October 29, 2026

4-(Piperidin-1-yl)phenol → HCID 21405650, compound

https://huagongshe.com/reaction/972890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Piperidin-1-yl)phenolHCID 90452—
ReactantEthyl bromophenylacetateHCID 97780—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 21405650HCID 21405650—

Reaction Steps

2.3 g. of sodium is dissolved in 100 ml. of absolute ethanol; 17.7 g. of 4-piperidinophenol is introduced into the solution, and then 24.3 g. of ethyl α-bromophenylacetate is added dropwise thereto and the mixture refluxed for 10 hours. The reaction mixture is then evaporated, the residue mixed with water, and the aqueous solution extracted with ethyl acetate. The ethyl acetate solution is washed twice with dilute KOH and twice with water, then dried, and the solvent is evaporated, thus obtaining the ethyl ester of α-phenyl-α-4-piperidinophenoxy-acetic acid; hydrochloride, m.p. 149°-151°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04053626
Source datasetuspto-grants-1977_10
ORD IDord-99c6fc8562064e6bad38c78bb67fceca
Source noteuspto-grants-1977_10