反应详情

A solution of 3-hydroxy-4-methoxyacetophenone (0.070 g, 0.421 mmol), (benzo[c][1,2,5]oxadiazol-5-yl)methoxyamine hydrochloride (0.126 g, 0.625 mmol) and pyridine (0.16 ml, 1.98 mmol) in ethanol (6 ml) was stirred at reflux under nitrogen for 4 h and cooled to room temperature. The solution was concentrated to a yellow oil which was diluted with water. The resultant suspension was extracted with dichloromethane (×3). The combined organic phases were washed with water, dried over magnesium sulphate, filtered and concentrated to a yellow oil. The crude product was purified by column chromatography (SiO2), eluting with 8:2 petrol/ethyl acetate, to give a slightly sticky solid which was further triturated with petroleum spirit (40-60°), to give 1-(3-hydroxy-4-methoxyphenyl)ethanone-O -[(benzo[c][1,2,5]oxadiazol-5-yl)methyl]oxime (CP9-33) as a light yellow solid (0.119 g, 90%).

1. temperatureat reflux under nitrogen for 4 h
2. concentrationThe solution was concentrated to a yellow oil which
3. additionwas diluted with water
4. extractionThe resultant suspension was extracted with dichloromethane (×3)
5. washThe combined organic phases were washed with water
6. dry with materialdried over magnesium sulphate
7. filtrationfiltered
8. concentrationconcentrated to a yellow oil
9. customThe crude product was purified by column chromatography (SiO2)
10. washeluting with 8:2 petrol/ethyl acetate
11. customto give a slightly sticky solid which
12. customwas further triturated with petroleum spirit (40-60°)