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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373012Generated: October 27, 2026

Potassium Iodide → 3-Methyl-5-[4-(4-phenyl-1-piperazinyl)butyl]-2-oxazolidinone

https://huagongshe.com/reaction/373012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Phenylpiperazinium chlorideHCID 75164—
Reactant5-(4-Chlorobutyl)-3-methyl-2-oxazolidinoneHCID 19811462—
Solvent1-ButanolHCID 263—
Product3-Methyl-5-[4-(4-phenyl-1-piperazinyl)butyl]-2-oxazolidinoneHCID 992698545%

Reaction Steps

A mixture of 5-(4-chlorobutyl)-3-methyl-2-oxazolidinone (10.0 g, 0.0524 mol), 1-phenylpiperazine hydrochloride (0.0524 mol, 10.39 g), potassium carbonate (28.94 g, 0.209 mol) and potassium iodide (1.0 g) was refluxed in 1-butanol (150 mL) for 24 hr and then stirred at room temperature for two days. The mixture was reheated to boiling and filtered hot. Methanolic hydrogen chloride was added to acidify the filtrate and addition of isopropyl ether caused a solid to precipitate. The solid was collected by filtration and dissolved in water. Potassium carbonate was added to make the solution basic and the product was extracted into two portions of ethyl acetate. The combined ethyl acetate layers were washed twice with water, three times with a saturated sodium bicarbonate solution and once with a saturated sodium chloride solution. The solution was dried (sodium sulfate), filtered, and evaporated under reduced pressure to an oil. Addition of isopropyl ether gave a solid which was recrystallized from isopropyl ether/methanol. The solid was collected by filtration, rinsed with light pet ether and dried under high vacuum to give 7.51 g (45% yield), mp 85°-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162322
Source datasetuspto-grants-1992_11
ORD IDord-87ff04457fcc4d198d001196dae5b14d
Source noteuspto-grants-1992_11