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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045036Generated: November 2, 2026

Potassium Carbonate → 4-(4-chlorophenyl)-1-methyl-1H-pyrazole-5-carbaldehyde

https://huagongshe.com/reaction/2045036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant4-bromo-1-methyl-1H-pyrazole-5-carbaldehydeHCID 2794634—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-(4-chlorophenyl)-1-methyl-1H-pyrazole-5-carbaldehydeHCID 86642504—

Reaction Conditions

Temperature45 °C

Reaction Steps

4-Bromo-1-methyl-1H-pyrazole-5-carbaldehyde (0.500 g), 4-chlorophenylboronic acid (0.455 g), tetrabutylammonium bromide (0.853 g), potassium carbonate (0.914 g) and palladium acetate (0.030 g) were stirred together in 5 mL of water and heated to 45° C. After stirring for 2.5 hours, the reaction was diluted with ethyl acetate (75 mL) and washed with water (25 mL), brine (50 mL), dried over magnesium sulfate, filtered and concentrated to give the crude material. The solid was chromatographed over silica gel (SF40-80) eluted using a gradient of 5% to 25% ethyl acetate/hexanes over 30 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586754B2
Source datasetuspto-grants-2013_11
ORD IDord-683d2a367c694c0faa9e0dd9ee91c664
Source noteuspto-grants-2013_11