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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212296Generated: October 25, 2026

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

https://huagongshe.com/reaction/2212296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
Reactant1-(2,3-Dichlorophenyl)ethan-1-oneHCID 91986—
ReactantAmmonium AcetateHCID 517165—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
Product2-Cyano-3-(2,3-dichlorophenyl)-but-2-enoic acid ethyl esterHCID 67073893—

Reaction Steps

A mixture of 2′,3′-dichloroacetophenone (50 mmole), ethyl cyanoacetate (50 mmole), 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 mmole), 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/petroleum ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101905B2
Source datasetuspto-grants-2006_09
ORD IDord-7755d8f1165f40bf9da510c5614e793f
Source noteuspto-grants-2006_09