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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1093597Erstellt: 25. Oktober 2026

Acetic Acid → HCID 178468617, Verbindung

https://huagongshe.com/reaction/1093597

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrazine hydrate (1:1)HCID 24654—
Edukt2,4-Dioxo-4-phenyl-butyric acid ethyl esterHCID 226503—
EduktSodium BicarbonateHCID 516892—
LösungsmittelWaterHCID 962—
ProduktHCID 178468617HCID 17846861788%

Reaktionsschritte

A solution of 2,4-dioxo-4-phenyl-butyric acid ethyl ester (1.68 g, 0.0076 mole), acetic acid (10 mL) and hydrazine hydrate (0.42 g, 0.0083 mole) was heated to reflux for 5 hours. The reaction mixture was then poured into iced water, basified with saturated aqueous NaHCO3 solution and the product was extracted with ethyl acetate. The ethyl acetate layer was collected and washed with brine solution, dried over sodium and concentrated under reduced pressure. The resulting residue was purified by column chromatography using basic aluminium oxide (50% ethyl acetate in hexane) to afford 1.442 g (88%) of 5-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester. LCMS: 217.09 (M+1)+, 97.92%. To a stirred solution of 5-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester (1.4 g, 0.00667 mol) in a mixture of THF (30 mL), methanol (15 mL) and H2O (10 mL) was added LiOH.H2O (0.839 g, 0.0199 mol) at ambient temperature. The resulting mixture was stirred at 45° C. overnight. Volatiles were evaporated and the residue was diluted with water, acidified with concentrated HCl solution and the product was extracted with ethyl acetate. The ethyl acetate layer was collected, dried over sodium sulfate and concentrated under reduced pressure to afford 1.26 g (86%) of 5-phenyl-1H-pyrazole-3-carboxylic acid. LCMS: 189.06 (M+1)+, 97.7%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08129376B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-13b8d5ceb1d947f8bec300bdc587e6de
Quellennotizuspto-grants-2012_03