تفاعل #2254164
ord-58b0274909c14fdcad918bf857f37136
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.ADDITIONwere added, at room temperature
- 2workup.DISTILLATIONThe solvent was distilled off under reduced pressure
- 3workup.ADDITIONWater was added to the residue and extraction with ethyl acetate
- 4غسيلThe organic layer was washed with a saturated aqueous sodium chloride solution
- 5تجفيفdried over anhydrous magnesium sulfate
- 6ترشيحfiltered
- 7أخرىto remove inorganic matter
- 8workup.DISTILLATIONThe solvent was distilled off under reduced pressure
- 9غسيلThe resulting crude crystal was washed with a 1:2 mixed solution of diisopropyl ether and n-hexane
الإجراء التجريبي
To a mixed solution of methanol (1.5 ml) and dimethyl sulfoxide (0.5 ml), of 0.50 g (2.94 mM) of the 3-amino-3-hydroxyimino-2-isopropoxyiminopropionitrile obtained in (1) of Example 1 were added, at room temperature, 0.73 g (6.4 mM) of a 30% aqueous hydrogen peroxide solution and 0.02 g (0.14 mM) of potassium carbonate. Stirring was conducted at room temperature for 4 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 residue and extraction with ethyl acetate was conducted. The organic layer 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 resulting crude crystal was washed with a 1:2 mixed solution of diisopropyl ether and n-hexane to obtain 0.35 g (yield: 63%) of the title compound.