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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270219Generated: October 30, 2026

Ethyl cyanoacetate → HCID 86607193, compound

https://huagongshe.com/reaction/270219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 68832755HCID 68832755—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
ProductHCID 86607193HCID 86607193—

Reaction Steps

A mixture of 4-(2-chloro-4-isopropylphenyl)but-3-en-2-one (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-b567572c433c4523b339c6e4ab96fcf7
Source noteuspto-grants-2008_11