반응 #64284

ord-dd1501b03a6249b1a7fd9157a965ee67

반응 방정식

CCCCCC
n-hexane
[H-].[Na+]
sodium hydride
CC1OC2(CCN(C)CC2)CC1=O
2,8-dimethyl-1-oxa-8-azaspiro[4,5]decan-3-one
C=C1CC2(CCN(C)CC2)OC1C
2,8-dimethyl-3-methylene-1-oxa-8-azaspiro[4,5]decane

반응 조건

온도
40°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척to wash off the oil component
  2. 2
    workup.DISTILLATIONthe remaining hexane was distilled off
  3. 3
    workup.ADDITIONDimethyl sulfoxide (8 ml) was added to the residue
  4. 4
    온도the mixture was heated at 60° to 70° C. for about one hour
  5. 5
    기타the faint-green solution thus obtained
  6. 6
    온도cooled
  7. 7
    기타giving a yellowish-red solution
  8. 8
    온도It was cooled to about 30° C.
  9. 9
    추출the resulting mixture was extracted with chloroform
  10. 10
    세척the extract was washed with saturated aqueous solution of sodium chloride
  11. 11
    건조dried over anhydrous magnesium sulfate
  12. 12
    workup.DISTILLATIONAfter distilling off the solvent under reduced pressure from the dried solution
  13. 13
    기타the residue was purified by silica gel column chromatography

실험 절차

60% oily sodium hydride (272 mg), placed in a flask, was treated with n-hexane in an argon gas atmosphere to wash off the oil component, and the remaining hexane was distilled off under reduced presure. Dimethyl sulfoxide (8 ml) was added to the residue, the mixture was heated at 60° to 70° C. for about one hour, the faint-green solution thus obtained was ice-cooled, and 2.43 g methyltriphenylphosphonium bromide was added. Heating the mixture at about 40° C. put the solid into solution, giving a yellowish-red solution. It was cooled to about 30° C., 590 mg 2,8-dimethyl-1-oxa-8-azaspiro[4,5]decan-3-one was added, and the mixture was stirred at room temperature for about two hours. It was then poured into 50 ml ice water, the resulting mixture was extracted with chloroform, and the extract was washed with saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. After distilling off the solvent under reduced pressure from the dried solution, the residue was purified by silica gel column chromatography by using, as eluent, a mixed solvent of chloroform/methanol (10:1 by volume), giving 320 mg of 2,8-dimethyl-3-methylene-1-oxa-8-azaspiro[4,5]decane as oil. It was dissolved in ether, and ethanolic hydrogen chloride was added to the solution, giving the corresponding hydrochloride as crystals.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05412096uspto-grants-1995_05