Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856828Generated: October 29, 2026

Sodium Carbonate → 5-Fluoro-1-(4-fluorophenyl)-2-(4-methylsulfonylphenyl)pyrrole

https://huagongshe.com/reaction/856828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantXenon difluorideHCID 83674—
Reactant1-(4-Fluorophenyl)-2-(4-methylsulfonylphenyl)pyrroleHCID 10829132—
ReactantHCID 178435160HCID 178435160—
SolventAcetonitrileHCID 6342—
Product5-Fluoro-1-(4-fluorophenyl)-2-(4-methylsulfonylphenyl)pyrroleHCID 2186278735.6%

Reaction Steps

0.90 g (2.7 mmol) of 1-(4-fluorophenyl)-2-(4-methylsulfonylphenyl)pyrrole (prepared as described in Example 33) was dissolved in 10 ml of acetonitrile in a reaction vessel made of polyethylene, and 0.46 g (2.7 mmol) of xenon difluoride was added to the resulting solution at 0° C., whilst stirring. The temperature of the reaction mixture was then allowed to return to room temperature, and the mixture was stirred at room temperature for 20 hours. At the end of this time, 20 ml of a saturated aqueous solution of sodium carbonate was added to the mixture, which was then extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium carbonate and then with water, after which it was dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure. The resulting residue was applied to a silica gel chromatography column and eluted with a 3:1 by volume mixture of hexane and ethyl acetate, to give 0.32 g of the title compound as white prismatic crystals (yield 34%), melting at 140-141° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039420E1
Source datasetuspto-grants-2006_12
ORD IDord-d63218da6254499d918725cef006e123
Source noteuspto-grants-2006_12