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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292801Generated: October 26, 2026

Water → 5-fluoro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde

https://huagongshe.com/reaction/1292801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium FluorideHCID 522689—
Reactant5-Chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehydeHCID 1478459—
SolventDimethyl SulfoxideHCID 679—
Product5-fluoro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehydeHCID 1975474766.4%

Reaction Conditions

Temperature130 °C

Reaction Steps

42.0 g (711.9 mmoles) of potassium fluoride was added to a solution of 60.4 g (282.7 mmoles) of 5-chloro-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboaldehyde dissolved in 700 ml of dimethyl sulfoxide. The mixture was stirred at 120 to 140° C. for 5 hours to give rise to a reaction. After confirmation of the completion of the reaction, the reaction mixture was poured into water, followed by extraction with ethyl acetate. The resulting organic layer was washed with water and an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein. The residue was purified by silica gel column chromatography (developing solvent: hexane-ethyl acetate mixed solvent) to obtain 36.8 g (yield: 66.0%) of 5-fluoro-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238689B2
Source datasetuspto-grants-2007_07
ORD IDord-11cea4e94f0540a686bfc31cac2313e2
Source noteuspto-grants-2007_07