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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270176Erstellt: 24. Oktober 2026

Ethyl cyanoacetate → Ethyl 3-(2-chlorophenyl)-2-cyanobut-2-enoate

https://huagongshe.com/de/reaction/270176

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl cyanoacetateHCID 7764—
EduktEthanone, 1-(2-chlorophenyl)-HCID 72864—
EduktAmmonium AcetateHCID 517165—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl 3-(2-chlorophenyl)-2-cyanobut-2-enoateHCID 67073569—

Reaktionsschritte

A mixture of 2′-chloroacetophenone (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 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-fd54da5602114e94950de7957523fde0
Quellennotizuspto-grants-2008_11