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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856832Generated: October 30, 2026

Sodium Carbonate → 1-(4-Fluorophenyl)-5-formyl-2-(4-methylsulfonylphenyl)pyrrole

https://huagongshe.com/reaction/856832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant1-(4-Fluorophenyl)-2-(4-methylsulfonylphenyl)pyrroleHCID 10829132—
SolventDimethylformamideHCID 6228—
Product1-(4-Fluorophenyl)-5-formyl-2-(4-methylsulfonylphenyl)pyrroleHCID 2186286650%

Reaction Conditions

Temperature60 °C

Reaction Steps

1.67 g (5.3 mmol) of 1-(4-fluorophenyl)-2-(4-methylsulfonylphenyl)pyrrole (prepared as described in Example 33) were dissolved in 30 ml of dimethylformamide, 0.50 ml (5.3 mmol) of phosphorous oxychloride was added to the resulting solution, and the mixture was then stirred at 60° C. for 2 hours. At the end of this time, the reaction mixture was gradually added to ice-water and the pH of the mixture was adjusted to a value of 8-9 by the addition of sodium carbonate. The mixture was then extracted with ethyl acetate. The organic extract was washed with water and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was applied to a silica gel chromatography column and eluted with a 5:1 by volume mixture of hexane and ethyl acetate, to give 0.90 g (yield 50%) of the title compound as a white powder, melting at 135-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039420E1
Source datasetuspto-grants-2006_12
ORD IDord-797c736b216b4f1a92a3c14702ef3a1d
Source noteuspto-grants-2006_12