تفاعل #2254165

ord-a140ce6aff4d4f5a827335f299bf6bd3

معادلة التفاعل

OO
hydrogen peroxide
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
OO
hydrogen peroxide
O=S([O-])([O-])=S.[Na+].[Na+]
sodium thiosulfate
OO
hydrogen peroxide
CC(C)ON=C(N)C(C#N)=NOC(C)C
3-amino-2,3-bis(isopropoxyimino)propionitrile
CC(C)ON=C(N)C(=NOC(C)C)C(N)=O
title compound
CC(C)ON=C(N)C(=NOC(C)C)C(N)=O
3-amino-2,3-bis(isopropoxyimino)propanamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGby stirring at room temperature for 3 hours
  2. 2
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  3. 3
    workup.ADDITIONWater was added to the resulting residue
  4. 4
    استخلاصfollowed by extraction with ethyl acetate
  5. 5
    أخرىThe organic layer obtained
  6. 6
    غسيلwas washed with a saturated aqueous sodium chloride solution
  7. 7
    تجفيفdried over anhydrous magnesium sulfate
  8. 8
    ترشيحfiltered
  9. 9
    أخرىto remove inorganic matter
  10. 10
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  11. 11
    أخرىThe crystal obtained
  12. 12
    غسيلwas 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.

المصدر

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