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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373018Generated: October 30, 2026

Potassium Iodide → 5-[4-[4-(2-Ethoxyphenyl)-1-piperazinyl]butyl]-3-methyl-2-oxazolidinone dihydrochloride

https://huagongshe.com/reaction/373018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Ethoxyphenyl)piperazine HydrochlorideHCID 12862418—
Reactant5-(2-Chlorobutyl)-3-methyl-2-oxazolidinoneHCID 19811487—
Solvent1-ButanolHCID 263—
Product5-[4-[4-(2-Ethoxyphenyl)-1-piperazinyl]butyl]-3-methyl-2-oxazolidinone dihydrochlorideHCID 1981146410%

Reaction Steps

Following the procedure of Example 5, a mixture of 5-(2-chlorobutyl)-3-methyl-2-oxazolidinone (5.2 g, 0.0272 mol), 1-(2-ethoxyphenyl)piperazine monohydrochloride (6.61 g, 0.0272 mol), potassium carbonate (15.05 g, 0.109 mol), and potassium iodide (1.0 g) in n-butanol (100 mL) gave an oil which was dissolved in a mixture of ethyl acetate/isopropyl ether/light pet ether (removing the impurities by filtration) and acidified with ethereal hydrogen chloride. The mixture was evaporated under reduced pressure and recrystallized once from isopropanol/methanol/isopropyl ether and then from isopropanol/isopropyl ether and dried under high vacuum at 60° C. to give 1.18 g (10% yield), mp 207°-212° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162322
Source datasetuspto-grants-1992_11
ORD IDord-b04914b1d39a4d11840f18a9192d366f
Source noteuspto-grants-1992_11