반응 #46112

ord-2ca94eb1bed54d7bbac7f53a2500c3d7

반응 방정식

Nc1cc(Cl)c(Cl)cc1F
4,5-Dichloro-2-fluoroaniline
O=S=O
sulphur dioxide
O=N[O-].[Na+]
sodium nitrite
CCOCC
ether
NS(=O)(=O)c1cc(Cl)c(Cl)cc1F
4,5-dichloro-2-fluorobenzenesulphonamide

반응 조건

온도
-5°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONThe resulting mixture is slowly added to suspension A and
  2. 2
    기타The ethereal phase is separated off
  3. 3
    세척washed with water (100 mL)
  4. 4
    농축The organic phase is concentrated to dryness by distillation under reduced pressure
  5. 5
    workup.DISSOLUTIONthe residue is re-dissolved in dioxane (25 mL)
  6. 6
    workup.ADDITIONThe solution is poured slowly
  7. 7
    workup.STIRRINGwhilst stirring, into a mixture of concentrated ammonia (25 mL) and water (10 mL)
  8. 8
    온도cooled on an ice bath
  9. 9
    workup.WAITAfter 30 minutes
  10. 10
    기타the solution is evaporated to dryness by distillation under reduced pressure
  11. 11
    기타the residue obtained
  12. 12
    workup.ADDITIONThe methanolic solution is treated with absorbent carbon
  13. 13
    여과filtered
  14. 14
    기타the filtrate is evaporated to dryness
  15. 15
    기타The residue is recrystallised from a methanol/water mixture

실험 절차

In a 500 mL round-bottom flask, a portion of glacial acetic acid (30 mL) is saturated for 30 minutes with a current of gaseous sulphur dioxide. To the resulting solution there is added a solution of cupric chloride (1.5 g) in water (10 mL) (suspension A). 4,5-Dichloro-2-fluoroaniline (5 g) is dissolved in a mixture of glacial acetic acid (30 mL) and concentrated hydrochloric acid (15 mL). The resulting solution is cooled to −5° C. on a bath of ice and salt. A solution of sodium nitrite (2.5 g) in water (10 mL) is then added dropwise with constant stirring. The resulting mixture is slowly added to suspension A and is stirred on an ice bath for 15 minutes. The mixture is then poured into a mixture of water (200 mL) and ether (200 mL). The ethereal phase is separated off and washed with water (100 mL). The organic phase is concentrated to dryness by distillation under reduced pressure and the residue is re-dissolved in dioxane (25 mL). The solution is poured slowly, whilst stirring, into a mixture of concentrated ammonia (25 mL) and water (10 mL) cooled on an ice bath. After 30 minutes, the solution is evaporated to dryness by distillation under reduced pressure and the residue obtained is dissolved in methanol. The methanolic solution is treated with absorbent carbon and filtered and the filtrate is evaporated to dryness. The residue is recrystallised from a methanol/water mixture.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741320B2uspto-grants-2010_06