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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463325Generated: October 27, 2026

Triethylene Glycol → 4-(4-Ethylphenoxy)piperidine

https://huagongshe.com/reaction/463325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylene GlycolHCID 8172—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantOxalateHCID 71081—
Reactant1-{4-[(Piperidin-4-yl)oxy]phenyl}ethan-1-oneHCID 13457427—
Product4-(4-Ethylphenoxy)piperidineHCID 1345742938.6%

Reaction Steps

A solution of 4-(4-acetylphenoxy)piperidine (liberated from 15.0 g, 48.5 mmol, of the oxalate), 7.45 g of potassium hydroxide, 5.39 ml of 85% hydrazine hydrate and 54 ml of triethyleneglycol was stirred at reflux for 1 hour. The mixture was then cooled to room temperature and the flask fitted with a distillation apparatus. The temperature was then raised to 190°-195° and water removed by distillation. The mixture was stirred at 190°-195° for 3 hours and the mixture allowed to cool to room temperature. The mixture was diluted with water, extracted twice with ether and with 1N HCl, made basic with saturated sodium carbonate, extracted with ether and dried over potassium carbonate. Filtration followed by evaporation of the solvent provided an oil. Kugelrohr distillation at 114°-116°/1 mm provided 3.84 g (18.7 mmol, 38.6%) of 4-(4-ethylphenoxy)piperidine, m.p. 37-41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518713
Source datasetuspto-grants-1985_05
ORD IDord-252253e7c675432f96f0686e96717777
Source noteuspto-grants-1985_05