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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59612Generated: October 26, 2026

Water → HCID 178493807, compound

https://huagongshe.com/reaction/59612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Carboxyphenylboronic acidHCID 2733957—
Reactant4-[(3-bromo-2-methoxyphenyl)hydrazinylidene]-2-(3,4-dimethylphenyl)-5-methylpyrazol-3-oneHCID 178486378—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventEthanolHCID 702—
ProductHCID 178493807HCID 178493807—

Reaction Steps

A mixture of 1-(3,4-dimethylphenyl)-3-methyl-4-(3-bromo-2-methoxyphenyl)hydrazono-5-pyrazolone (5 g) prepared as in Example 2, and 3-carboxyphenylboronic acid (2.99 g), bis(triphenylphosphine)palladium(II)chloride [PdCl2(PPh3)2] (0.42 g), potassium hydroxide (1.74 g) in ethanol. (250 mL) and water (30 mL) was heated to about reflux temperature and stirred for about 24 hours. The hot mixture was filtered to remove the catalyst. The clear filtrate was concentrated under vacuum. To the residue, water (100 mL) was added; acidified to pH 3-5 using hydrochloric acid and stirred for about 30 minutes at about room temperature. The slurry was filtered to give a yellowish orange solid product, which was washed with water (50 mL) and dried in an oven at about 55° C. to about 60° C. for about 12 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440927B2
Source datasetuspto-grants-2016_09
ORD IDord-8d908f82a67948d084d40fd3232b94ae
Source noteuspto-grants-2016_09