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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415768Generated: October 28, 2026

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

https://huagongshe.com/reaction/1415768

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 numberUS05908858
Source datasetuspto-grants-1999_06
ORD IDord-69481f5ca3c64a0d98308cd79adb7d12
Source noteuspto-grants-1999_06