تفاعل #2254165
ord-a140ce6aff4d4f5a827335f299bf6bd3
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 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
- 4استخلاصfollowed by extraction with ethyl acetate
- 5أخرىThe organic layer obtained
- 6غسيلwas washed with a saturated aqueous sodium chloride solution
- 7تجفيفdried over anhydrous magnesium sulfate
- 8ترشيحfiltered
- 9أخرىto remove inorganic matter
- 10workup.DISTILLATIONThe solvent was distilled off under reduced pressure
- 11أخرىThe crystal obtained
- 12غسيلwas washed with a 1:2 mixed solution of diisopropyl ether and n-hexane
الإجراء التجريبي
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.