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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253662Generated: November 3, 2026

Potassium Iodide → HCID 15158294, compound

https://huagongshe.com/reaction/2253662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2H-1,3-Benzodioxol-5-yl)piperidin-4-olHCID 15034715—
ReactantHCID 15117120HCID 15117120—
SolventAcetonitrileHCID 6342—
ProductHCID 15158294HCID 15158294—

Reaction Steps

4.10 g of 5-(2-methanesulfonyloxyethyl)-3-p-methoxyphenyloxazolidin-2-one [m.p. 61°-64°; obtainable by reaction of 3,4-epoxy-1-butanol with N-benzyl-p-methoxyaniline to give 1-(N-benzyl-p-methoxyanilino)butane-2,4-diol (resin), hydrogenolysis to give 1-p-methoxyanilinobutane-2,4-diol (resin), reaction with diethyl carbonate to give 5-(2-hydroxyethyl)-3-p-methoxyphenyloxazolidin-2-one (m.p. 77°-78°) and reaction with CH3SO2Cl] are boiled together with 3.13 g of 4-hydroxy-4-(3,4-methylenedioxyphenyl)piperidine ("M"), 2.16 g of potassium iodide and 1.8 g of potassium carbonate in 100 ml of acetonitrile for 16 hours, the mixture is cooled, worked up as usual, to give 5-[2-(4-hydroxy-4-(3,4-methylenedioxyphenyl)piperidino)ethyl]-3-p-methoxyphenyloxazolidin-2-one, m.p. 128°-130°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05232931
Source datasetuspto-grants-1993_08
ORD IDord-17df9c6ce56546d28f68b963bf97a050
Source noteuspto-grants-1993_08