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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59620Generated: October 28, 2026

Potassium Hydroxide → HCID 178433881, compound

https://huagongshe.com/reaction/59620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant3-Carboxyphenylboronic acidHCID 2733957—
ReactantHCID 178433874HCID 178433874—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178433881HCID 178433881—

Reaction Steps

A mixture of 1-(3,4-dimethylphenyl)-3-methyl-4-(3-bromo-2-hydroxyphenyl)hydrazono-5-pyrazolone (2 g) prepared as in Example 10, 3-carboxyphenylboronic acid (1 g), bis(triphenylphosphine)palladium(II)chloride [PdCl2(PPh3)2] (0.2 g), potassium hydroxide (1.50 g) in ethanol (50 mL) and water (20 mL) was heated to about reflux temperature and stirred for about 20 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 an orange solid, which was washed with water (20 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-2a89935dcc5a419bb179a36f059842e9
Source noteuspto-grants-2016_09