Reacción #357345
ord-2cbe06d157694f0eb7719a4485f3438d
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturato reflux in a Dean-Stark apparatus
- 2workup.WAITAfter an additional 10 hours
- 3Lavadowashed with water (240 mL), brine (40 mL)
- 4Otrodried (Na2S04)
- 5FiltraciónAfter filtering
- 6Concentraciónthe extract was concentrated in vacuo
- 7workup.ADDITIONthe desired product, as a mixture of E and Z-isomers
- 8Otrowas isolated by column chromatography on silica gel
- 9Lavadoeluting with 5% ethyl acetate in petroleum ether
- 10Otroaffording an oil that
- 11Otroon standing at room temperature
Procedimiento
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.