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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270163Generated: October 30, 2026

Acetophenone → Ethyl 2-cyano-3-phenyl-2-butenoate

https://huagongshe.com/reaction/270163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
ReactantEthyl cyanoacetateHCID 7764—
ReactantAmmonium AcetateHCID 517165—
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-cyano-3-phenyl-2-butenoateHCID 29024—

Reaction Steps

A mixture of acetophenone (50 mmol), ethyl cyanoacetate (50 mmol), acetic; acid (1.14 mL), ammonium acetate (400 mg), and benzene (50 mL) was 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 mL) are added. After an additional 10 hours, the reaction was cooled to room temperature, diluted with ethyl acetate (30 mL), washed with water (240 mL), brine (40 mL), and dried (Na2S04). After filtering, the extract was concentrated in vacuo and the desired product, as a mixture of E and Z-isomers, was isolated by column chromatography on silica gel, eluting with 5% ethyl acetate in petroleum ether, affording an oil that solidified on standing at room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449490B2
Source datasetuspto-grants-2008_11
ORD IDord-2cbe06d157694f0eb7719a4485f3438d
Source noteuspto-grants-2008_11