반응 #2254165

ord-a140ce6aff4d4f5a827335f299bf6bd3

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  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
    추출followed by extraction with ethyl acetate
  5. 5
    기타The organic layer obtained
  6. 6
    세척was washed with a saturated aqueous sodium chloride solution
  7. 7
    건조dried over anhydrous magnesium sulfate
  8. 8
    여과filtered
  9. 9
    기타to remove inorganic matter
  10. 10
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  11. 11
    기타The crystal obtained
  12. 12
    세척was 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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09044013B2uspto-grants-2015_06