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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212315Generated: October 26, 2026

Ethyl cyanoacetate → 2-Cyano-4,4-bis(ethoxycarbonyl)-3-methyl-4-phenyl-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/2212315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantAmmonium AcetateHCID 517165—
ReactantDiethyl 2-acetyl-2-phenylmalonateHCID 21964398—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
Product2-Cyano-4,4-bis(ethoxycarbonyl)-3-methyl-4-phenyl-but-2-enoic acid ethyl esterHCID 68831464—

Reaction Steps

A mixture of diethyl 2-acetyl-2-phenylmalonate (50 mmole, Example 32, Part A), 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-246cae98ae22484495b20d1683e6297e
Source noteuspto-grants-2006_09