HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59620Generated: October 28, 2026
Potassium Hydroxide → HCID 178433881, compound
https://huagongshe.com/reaction/59620
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Carboxyphenylboronic acid | HCID 2733957 | — |
| Reactant | HCID 178433874 | HCID 178433874 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178433881 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440927B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-2a89935dcc5a419bb179a36f059842e9 |
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| Source note | uspto-grants-2016_09 |
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