反应详情

A mixture of 2-(3-benzoylphenyl)-2-(hydroxyimino)acetonitrile (14.5 g), 4N aqueous solution of potassium hydroxide (80 ml) and ethanol (80 ml) was heated under reflux for 20 hours. The reaction mixture was cooled to room temperature, 1N hydrochloric acid was added to make the solution acidic and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was dissolved in ethanol (150 ml) and concentrated sulfuric acid (catalytic amount) was added. The reaction mixture was heated under reflux for 15 hours, cooled to room temperature, poured into an aqueous saturated solution of sodium bicarbonate and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography to obtain ethyl Z-2-(3-benzoylphenyl)-2-(hydroxyimino)acetate (2.48 g, yield 14%) as a pale-brown oil from an ethyl acetate-hexane (1:2, v/v)-eluted fraction.

1. temperaturewas heated
2. temperatureunder reflux for 20 hours
3. extractionextracted with ethyl acetate
4. washThe ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride
5. dry with materialdried (MgSO4)
6. concentrationconcentrated
7. dissolutionThe residue was dissolved in ethanol (150 ml)
8. additionconcentrated sulfuric acid (catalytic amount) was added
9. temperatureThe reaction mixture was heated
10. temperatureunder reflux for 15 hours
11. temperaturecooled to room temperature
12. additionpoured into an aqueous saturated solution of sodium bicarbonate
13. extractionextracted with ethyl acetate
14. washThe ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride
15. dry with materialdried (MgSO4)
16. concentrationconcentrated