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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270223Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/270223

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl cyanoacetateHCID 7764—
EduktAmmonium AcetateHCID 517165—
EduktDiethyl 2-acetyl-2-phenylmalonateHCID 21964398—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Cyano-4,4-bis(ethoxycarbonyl)-3-methyl-4-phenyl-but-2-enoic acid ethyl esterHCID 68831464—

Reaktionsschritte

A mixture of diethyl 2-acetyl-2-phenylmalonate (50 mmol, Example 32, Part A), 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07449490B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-c28115e71d7444098406030b7be2bd55
Quellennotizuspto-grants-2008_11