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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30701Erstellt: 25. Oktober 2026

Water → (2e)-3-[5-(4-Fluorophenyl)-1-methyl-1h-pyrazol-4-yl]but-2-enoic acid

https://huagongshe.com/reaction/30701

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTetrahydrofuranHCID 8028—
EduktAmmonium ChlorideHCID 25517—
Edukt5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehydeHCID 23157484—
EduktHCID 178418573HCID 178418573—
LösungsmittelIsopropanolHCID 3776—
Produkt(2e)-3-[5-(4-Fluorophenyl)-1-methyl-1h-pyrazol-4-yl]but-2-enoic acidHCID 69207641—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a mixture of 5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde (4.50 g) and tetrahydrofuran (50 ml) was added dropwise methyl magnesium bromide (1 mol/L tetrahydrofuran solution, 25 ml) at 0° C. and the mixture was stirred at 0° C. for 30 min. The reaction mixture was poured into a saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate and concentrated and the residue was dissolved in acetone (60 ml). This solution was cooled to 0° C. and the Jones reagent (prepared by the method described in New Courses in Experiment Chemistry, Vol. 15, p. 151, published by Maruzen Company, Limited) was added dropwise until the red color of the reagent no longer disappeared. Isopropyl alcohol and water were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate and concentrated. The residue was dissolved in N,N-dimethylformamide (50 ml). To this solution were added ethyl diethylphosphonoacetate (6.0 g) and sodium hydride (60% in oil, 1.0 g) and the mixture was stirred at 80° C. for 12 hrs. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate, concentrated and the residue was purified by silica gel column chromatography to give a yellow oil from a fraction eluted with ethyl acetate-hexane (1:1, v/v). This yellow oil was dissolved in a mixture of acetic acid-37% hydrochloric acid (20-20 ml) and the mixture was stirred at 120° C. for 3 hrs. The reaction mixture was concentrated and poured into water. The precipitated crystals were collected by filtration, washed with water and dried to give (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]but-2-enoic acid. (4.60 g, 80%) as colorless crystals. Recrystallization thereof from ethyl acetate-hexane gave colorless prism crystals. melting point: 123-124° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423159B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-ce6f6ffa46ad480d826895a396748b2d
Quellennotizuspto-grants-2008_09