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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30674Erstellt: 24. Oktober 2026

Malonic Acid → (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acid

https://huagongshe.com/de/reaction/30674

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMalonic AcidHCID 867—
EduktPiperidineHCID 8082—
EduktSodium HydroxideHCID 14798—
Edukt5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehydeHCID 23157484—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiglymeHCID 8150—
Produkt(2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acidHCID 6920898190%

Reaktionsbedingungen

Temperatur92.5 °C

Reaktionsschritte

To a mixture of 5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde (3.00 g), malonic acid (1.99 g) and bis(2-methoxyethyl) ether (9 mL) was added dropwise piperidine (1.89 mL) over about 10 min. The mixture was stirred at 90-95° C. for 1 hr. and further at 105-110° C. for 4 hrs. After cooling to 25° C., toluene (12 mL) and 1N aqueous sodium hydroxide solution (15 mL) were added and the mixture was stirred. The aqueous layer was separated and the organic layer was extracted with 1N aqueous sodium hydroxide solution (6 mL). The aqueous layers were combined and washed with toluene. The layers were adjusted to pH 3.5-4.0 with 2N hydrochloric acid at 20-30° C. and water (9 mL) was added dropwise. After stirring at 25° C. for 1 hr., the precipitated crystals were collected by filtration and washed with 20% ethanol to give (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acid (3.24 g, yield 90%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423159B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-db6aa61893614edf9ca87b9570f1139c
Quellennotizuspto-grants-2008_09