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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807377Generated: October 31, 2026

Potassium Carbonate → HCID 50997448, compound

https://huagongshe.com/reaction/1807377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,4-Dichlorobenzeneboronic acidHCID 2734330—
ReactantHCID 50997446HCID 50997446—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 50997448HCID 5099744860%

Reaction Steps

To a stirred solution of 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid [1-(3-iodo-phenyl)-ethyl]-methoxy-amide (0.2 g, 0.46 mmol), prepared as described in example P2, in a mixture of ethanol (12 ml) and water (4 ml) was added, 3,4-dichloro-phenyl boronic acid (0.096 g, 0.5 mmol) followed by palladium acetate (0.052 g, 0.23 mmol) and potassium carbonate (0.19 g, 1.38 mmol). It was stirred for 18 hours at ambient temperature. Reaction mass was filtered on celite bed then diluted with water and extracted in ethyl acetate (3×60 ml), washed with water, brine and dried over anhydrous sodium sulfate). The crude mass was purified by column chromatography using 36% Ethyl acetate in hexane to yield 0.12 g (60% of theory) of 3-Difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid [1-(3′,4′-dichloro-biphenyl-3-yl)-ethyl]-methoxy-amide in form of a solid. Mp 162-164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357634B2
Source datasetuspto-grants-2013_01
ORD IDord-95fc2081226944db9bcf77998e4547ad
Source noteuspto-grants-2013_01