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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59626Erstellt: 24. Oktober 2026

Methane → HCID 178493807, Verbindung

https://huagongshe.com/de/reaction/59626

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
EduktHydrochloric AcidHCID 313—
EduktPotassium HydroxideHCID 14797—
Edukt3-Carboxyphenylboronic acidHCID 2733957—
Edukt4-[(3-bromo-2-methoxyphenyl)hydrazinylidene]-2-(3,4-dimethylphenyl)-5-methylpyrazol-3-oneHCID 178486378—
KatalysatorDichlorobis(triphenylphosphine)palladiumHCID 6102075—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 178493807HCID 178493807—

Reaktionsschritte

A mixture of 1-(3,4-dimethylphenyl)-3-methyl-4-(3-bromo-2-methoxyphenyl)hydrazono-5-pyrazolone (10 g) prepared as in Example 16, 3-carboxyphenylboronic acid (5.2 g), bis(triphenylphosphine)palladium(II)chloride [PdCl2(PPh3)2] (0.84 g), potassium hydroxide (6.72 g) in ethanol (200 mL) and water (15 mL) was heated to about reflux temperature under nitrogen atmosphere and stirred for about 8 hours. The reaction mixture was cooled to about 30° C. to about 35° C. and stirred for about 4 hours at about the same temperature. The reaction mixture was treated with Norit™ charcoal and filtered over celite bed. The filtrate was treated with EDTA and Scavenger Type 2S. The mixture was stirred at about 30° C. to about 40° C. for about 20 hours and filtered over celite bed. To the filtrate, hydrochloric acid was added to adjust the pH to about 3 to about 5. The mixture was stirred for about 2 hours at about 80° C. to about 85° C. The mixture was cooled to about 40° C. to about 45° C. and filtered. The wet cake was treated with potassium hydroxide in methanol and stirred to give a clear solution. The solution was treated with 50% tributylphosphene in ethyl acetate and stirred for about 20 hours at about room temperature. The pH of the solution was adjusted to about 2 to about 4 using hydrochloric acid and the solid obtained was filtered and purified using tetrahydrofuran. Yield: 9.3 g

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440927B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-65b5635ca16c4361ba1b694ba355eb5c
Quellennotizuspto-grants-2016_09