반응 #77489

ord-62c7c866bd5f45e0af5784edde849ebc

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The precipitate is filtered off
  2. 2
    농축the filtrate concentrated by evaporation on a RE
  3. 3
    기타The residue of evaporation
  4. 4
    workup.DISSOLUTIONis dissolved in 4 l of EtOAc
  5. 5
    기타4 l of water, the water phase is separated
  6. 6
    추출extracted twice with EtOAc
  7. 7
    세척The organic phases are washed with water, 0.1 N HCl, water, sat. Na2CO3, water and brine
  8. 8
    건조dried (Na2SO4)
  9. 9
    농축concentrated by evaporation
  10. 10
    workup.STIRRINGStirring of the residue in 2.5 l of hexane
  11. 11
    여과filtering

실험 절차

470 ml (4.28 mol) of N-methylmorpholine, followed by 224 ml (2.98 mol) of allylamine are added under ice cooling to 750 g (2.81 mol) of 2-iodo-benzoic acid chloride in 7.5 l of acetonitrile, and stirred for 60 min at RT. The precipitate is filtered off and the filtrate concentrated by evaporation on a RE. The residue of evaporation is dissolved in 4 l of EtOAc and 4 l of water, the water phase is separated and extracted twice with EtOAc. The organic phases are washed with water, 0.1 N HCl, water, sat. Na2CO3, water and brine, dried (Na2SO4) and concentrated by evaporation. Stirring of the residue in 2.5 l of hexane and filtering yields 2-iodo-benzoic acid allylamide; m.p. 105-106° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06706731B2uspto-grants-2004_03