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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130606Erstellt: 25. Oktober 2026

3-(2,4-Difluorophenyl)acrylic Acid → 3-(2,4-difluorophenyl)propanoic Acid

https://huagongshe.com/reaction/130606

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(2,4-Difluorophenyl)acrylic AcidHCID 603502—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
Produkt3-(2,4-difluorophenyl)propanoic AcidHCID 498639590%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

The procedure was as in Example 5, but the 2,4-difluorocinnamic acid obtained was not isolated. The aqueous-acidic product suspension obtained was treated with 2 g of Pd/C (5% strength) at 50° C. with further stirring and heated to 100° C. It was then pressurized to 5 bar of hydrogen. After constant pressure had been achieved, it was cooled to room temperature, the pressure was released and the solid was filtered off. The filter cake was taken up in methylene chloride, the palladium catalyst was filtered off and the solvent was removed. After drying in vacuo, 100.5 g of 3-(2,4-difluorophenyl)propionic acid (90% of theory; melting point: 100° C.) were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381832B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-668b816b464443888318838bbd96957b
Quellennotizuspto-grants-2008_06