تفاعل #2254164

ord-58b0274909c14fdcad918bf857f37136

معادلة التفاعل

O=C([O-])[O-].[K+].[K+]
potassium carbonate
OO
hydrogen peroxide
O=S([O-])([O-])=S.[Na+].[Na+]
sodium thiosulfate
CC(C)ON=C(C#N)C(N)=NO
3-amino-3-hydroxyimino-2-isopropoxyiminopropionitrile
CC(C)ON=C(N)C(C#N)=NOC(C)C
( 1 )
CC(C)ON=C(N)C(C#N)=NOC(C)C
3-amino-2,3-bis(isopropoxyimino)propionitrile
OO
hydrogen peroxide
CC(C)ON=C(C(N)=O)C(N)=NO
title compound
المردود 63.0%
CC(C)ON=C(C(N)=O)C(N)=NO
3-amino-3-hydroxyimino-2-isopropoxyiminopropanamide
المردود 63.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added, at room temperature
  2. 2
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  3. 3
    workup.ADDITIONWater was added to the residue and extraction with ethyl acetate
  4. 4
    غسيلThe organic layer was washed with a saturated aqueous sodium chloride solution
  5. 5
    تجفيفdried over anhydrous magnesium sulfate
  6. 6
    ترشيحfiltered
  7. 7
    أخرىto remove inorganic matter
  8. 8
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  9. 9
    غسيلThe 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09044013B2uspto-grants-2015_06