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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212257Generated: October 25, 2026

Ethyl cyanoacetate → 2-Cyano-3-(3-methylphenyl)-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/2212257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
Reactant3-MethylacetophenoneHCID 11455—
ReactantAmmonium AcetateHCID 517165—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
Product2-Cyano-3-(3-methylphenyl)-but-2-enoic acid ethyl esterHCID 297786—

Reaction Steps

A mixture of 3′-methylacetophenone (50 mmole), ethyl cyanoacetate (50 mmole), acetic acid (1.14 mL) ammonium acetate (400 mg), and benzene (50 mL) was heated to reflux in a Dean-Stark apparatus. After approximately 10 hours, additional ethyl cyanoacetate (50 mmole), acetic acid (1.14 mL), and ammonium acetate (400 mg) are added. After an additional 10 hours, the reaction was 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 was concentrated in vacuo and the desired product, as a mixture of E- and Z-isomers, was isolated by column chromatography on silica gel, eluting with 5% ethyl acetate/petroleum ether. The purified oil solidified on standing at room tempera-ture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101905B2
Source datasetuspto-grants-2006_09
ORD IDord-51037baff34b4c6a93219cef0f9aa86f
Source noteuspto-grants-2006_09