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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533929Generated: November 3, 2026

Potassium Iodide → 3-Methyl-5-(4-Phenyl-1-Piperazinylmethyl)-2-Oxazolidinone

https://huagongshe.com/reaction/1533929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-PhenylpiperazineHCID 7096—
ReactantSodium CarbonateHCID 10340—
Reactant5-(Chloromethyl)-3-methyl-2-oxazolidinoneHCID 12889925—
Solvent1-ButanolHCID 263—
Product3-Methyl-5-(4-Phenyl-1-Piperazinylmethyl)-2-OxazolidinoneHCID 1503009716.3%

Reaction Steps

This compound was prepared according to the procedure of Example 2. A mixture of 3.2 g (0.02 mol) of 1-phenylpiperazine, 3.0 g (0.02 mol) of 5-(chloromethyl)-3-methyl-2-oxazolidinone, 8.0 g (0.075 mol) of anhydrous sodium carbonate, and 0.4 g of potassium iodide in 100 mL of 1-butanol gave a brown oil as residue. The oil was converted to the dioxalate and the solid was recrystallized from acetonitrile-dimethylformamide but did not give a correct combustion analysis. The salt was partitioned between methylene chloride and a 4% sodium hydroxide solution. The organic layer was dried (Na2SO4) and concentrated to yield 0.9 g (16%) of white solid, mp 110°-112° C. (2-propanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05086055
Source datasetuspto-grants-1992_02
ORD IDord-2ad6af93b3db4b0e8d0bbbbabe3db175
Source noteuspto-grants-1992_02