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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607891Generated: November 2, 2026

Potassium Iodide → 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-[bis(4-fluorophenyl)methyl]piperazine

https://huagongshe.com/reaction/1607891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
Reactant1-[Bis(4-fluorophenyl)methoxy]-2-chloroethaneHCID 10779302—
SolventMethyl Isobutyl KetoneHCID 7909—
Product1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-[bis(4-fluorophenyl)methyl]piperazineHCID 5196089—

Reaction Steps

A mixture containing 12.7 g of 2-[bis(4-fluorophenyl)methoxy]ethyl chloride, 8.6 g of 1-[bis(4-fluorophenyl)methyl]piperazine, 6.2 g of powdered anhydrous potassium carbonate and 0.5 g of potassium iodide in 90ml of methyl isobutyl ketone is refluxed for 20 hours while stirring. Aftercooling down, the mixture is evaporated under reduced pressure and water and ethyl ether are added to the residue. The ethereal phase is washed with water, dried over anhydrous magnesium sulfate and evaporated. The crude product is purified on a Kieselgel column by using a 2:1 mixture of benzene and chloroform as eluant. The appropriate fractions are combined, evaporated and the residue is recrystallized from ethanol to give the aimed compound, m.p.: 87°-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868184
Source datasetuspto-grants-1989_09
ORD IDord-daba2ca34f844701a9eaf88308ab45cc
Source noteuspto-grants-1989_09