반응 #2254165
ord-a140ce6aff4d4f5a827335f299bf6bd3
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후처리
- 1workup.STIRRINGby stirring at room temperature for 3 hours
- 2workup.DISTILLATIONThe solvent was distilled off under reduced pressure
- 3workup.ADDITIONWater was added to the resulting residue
- 4추출followed by extraction with ethyl acetate
- 5기타The organic layer obtained
- 6세척was washed with a saturated aqueous sodium chloride solution
- 7건조dried over anhydrous magnesium sulfate
- 8여과filtered
- 9기타to remove inorganic matter
- 10workup.DISTILLATIONThe solvent was distilled off under reduced pressure
- 11기타The crystal obtained
- 12세척was washed with a 1:2 mixed solution of diisopropyl ether and n-hexane
실험 절차
To a methanol solution (140 ml) of 29.0 g (137 mM) of 3-amino-2,3-bis(isopropoxyimino)propionitrile were added, at room temperature, 47 g (415 mM) of a 30% aqueous hydrogen peroxide solution, 1.5 g (15 mM) of sodium carbonate and 2.3 g (7.1 mM) of tetrabutylammonium bromide. Stirring was conducted at room temperature for 4 hours. Since the raw materials remained, further 24 g (212 mM) of a 30% aqueous hydrogen peroxide solution was added, followed by stirring at room temperature for 3 hours. Excessive hydrogen peroxide was treated with an aqueous sodium thiosulfate solution. The solvent was distilled off under reduced pressure. Water was added to the resulting residue, followed by extraction with ethyl acetate. The organic layer obtained was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered to remove inorganic matter. The solvent was distilled off under reduced pressure. The crystal obtained was washed with a 1:2 mixed solution of diisopropyl ether and n-hexane to obtain 29.0 g (yield: 92%) of the title compound.