Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270193Generated: October 26, 2026

Ethyl cyanoacetate → ethyl 2-cyano-3-(2-methoxyphenyl)but-2-enoate

https://huagongshe.com/reaction/270193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
Reactant2'-MethoxyacetophenoneHCID 68481—
ReactantAmmonium AcetateHCID 517165—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
Productethyl 2-cyano-3-(2-methoxyphenyl)but-2-enoateHCID 4270494—

Reaction Steps

A mixture of 2′-methoxyacetophenone (50 mmol), ethyl cyanoacetate (50 mmol), acetic acid (1.14 mL) ammonium acetate (400 mg), and benzene (50 mL) is heated to reflux in a Dean-Stark apparatus. After approximately 10 hours, additional ethyl cyanoacetate (50 mmol), acetic acid (1.14 mL), and ammonium acetate (400 mg) are added. After an additional 10 hours, the reaction is cooled to room temperature, diluted with ethyl acetate (30 mL), washed with water (240 mL), brine (40 mL), and dried (Na2SO4). After filtering, the extract is concentrated in vacuo and the desired product, as a mixture of E and Z-isomers, is isolated by column chromatography on silica gel, eluting with 5% ethyl acetate in petroleum ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449490B2
Source datasetuspto-grants-2008_11
ORD IDord-4d32cdb799c7458a9ab21113ad49daaa
Source noteuspto-grants-2008_11