반응 #77489
ord-62c7c866bd5f45e0af5784edde849ebc
반응 조건
상세 조건
See reaction.notes.procedure_details.
후처리
- 1여과The precipitate is filtered off
- 2농축the filtrate concentrated by evaporation on a RE
- 3기타The residue of evaporation
- 4workup.DISSOLUTIONis dissolved in 4 l of EtOAc
- 5기타4 l of water, the water phase is separated
- 6추출extracted twice with EtOAc
- 7세척The organic phases are washed with water, 0.1 N HCl, water, sat. Na2CO3, water and brine
- 8건조dried (Na2SO4)
- 9농축concentrated by evaporation
- 10workup.STIRRINGStirring of the residue in 2.5 l of hexane
- 11여과filtering
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.