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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66483Erstellt: 24. Oktober 2026

Ethyl Acrylate → 4-Oxo-4-(thiophen-3-yl)butanoic acid

https://huagongshe.com/de/reaction/66483

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcrylateHCID 8821—
EduktPotassium HydroxideHCID 14797—
Edukt3-ThiophenecarboxaldehydeHCID 68135—
Edukt4-Morpholinyl(3-thienyl)acetonitrileHCID 13041699—
LösungsmittelEthanolHCID 702—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Oxo-4-(thiophen-3-yl)butanoic acidHCID 315657—

Reaktionsschritte

As for Example 6, 99 g. of 3-thiophenecarboxaldehyde is converted to α-(3-thienyl)-4-morpholineacetonitrile (137 g.; m.p. 85°-87° C.). The preceding compound 50.5 g. is reacted with 100 ml. of ethyl acrylate in 500 ml. of tetrahydrofuran in the presence of 50 ml. of 30% potassium hydroxide in ethanol. The solvent is removed from the reaction mixture and the residue is heated with 6 N hydrochloric acid to give 3-(3-thenoyl)propionic acid. As for Example 1, the preceding compound is converted to the product of the Example to give a glass.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04342689
Quelldatensatzuspto-grants-1982_08
ORD IDord-b323d8b8969a4f969af3b89e62aa45ea
Quellennotizuspto-grants-1982_08