Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155022Generated: October 25, 2026

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

https://huagongshe.com/reaction/1155022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantPotassium HydroxideHCID 14797—
Reactant3-ThiophenecarboxaldehydeHCID 68135—
Reactant4-Morpholinyl(3-thienyl)acetonitrileHCID 13041699—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product4-Oxo-4-(thiophen-3-yl)butanoic acidHCID 315657—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04299769
Source datasetuspto-grants-1981_11
ORD IDord-db7445088109459db09f44bb449fdf0c
Source noteuspto-grants-1981_11