반응 #320465

ord-e61f7be9d7924046bc7d0b79ad900d0d

반응 방정식

C=CC#N
acrylonitrile
Br
HBr
Cc1oc(-c2ccccc2)nc1CCOc1ccc(N)cn1
5-amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine
O=N[O-].[Na+]
sodium nitrite
Cc1oc(-c2ccccc2)nc1CCOc1ccc(CC(Br)C#N)cn1
2-bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrile
수율 48.0%

반응 조건

온도
10°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타exceeding 10° C.
  2. 2
    workup.ADDITIONTo the mixture was added
  3. 3
    workup.STIRRINGwhile stirring vigorously
  4. 4
    workup.STIRRINGThe reaction mixture was stirred for further one hour at temperature
  5. 5
    기타ranging from 30° to 35° C.
  6. 6
    농축followed by concentration under reduced pressure
  7. 7
    workup.ADDITIONThe concentrate was poured into water, which
  8. 8
    추출followed by extraction with ethyl acetate
  9. 9
    세척The ethyl acetate layer was washed with water
  10. 10
    건조dried (MgSO4)
  11. 11
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  12. 12
    세척From the fractions eluted with ethyl acetate--hexane (1:1

실험 절차

To a mixture of 5-amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine (9.1 g), an aqueous solution of HBr (47%, 14.2 ml) and acetone (150 ml) was added dropwise, at temperature not exceeding 10° C. a solution of sodium nitrite (NaNO2) (2.33 g) in water (10 ml). The mixture was stirred for 30 minutes at 10° C., to which was added acrylonitrile (CH2 =CHCN) (12.1 ml). To the mixture was added, while stirring vigorously, copper(I) oxide (Cu2O) (0.1 g). The reaction mixture was stirred for further one hour at temperature ranging from 30° to 35° C., followed by concentration under reduced pressure. The concentrate was poured into water, which was made alkaline with a conc. ammonia water, followed by extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), then the solvent was distilled off under reduced pressure. The residual oily product was subjected to a silica gel column chromatography. From the fractions eluted with ethyl acetate--hexane (1:1, v/v), was obtained 2-bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrile (6.11 g, 48%), which was recrystallized from ethyl acetate--hexane to give colorless crystals, m.p.93°-94° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05591862uspto-grants-1997_01