反応 #4330

ord-3dbdfcae709944628a41bf0158fca242

反応方程式

Cl
hydrochloric acid
Nc1cc(F)ccc1F
2,5-difluoroaniline
c1ccncc1
pyridine
O=S(=O)(Cl)c1ccccc1
benzenesulphonyl chloride
O=S(=O)(Nc1cc(F)ccc1F)c1ccccc1
2,5-difluoro-N-benzenesulphonylaniline

溶媒

反応条件

温度
40°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他is between 35° C. and 45° C
  2. 2
    workup.ADDITIONafter the addition
  3. 3
    workup.ADDITIONhave been added
  4. 4
    その他The expected product precipitates
  5. 5
    ろ過After filtration
  6. 6
    洗浄washing
  7. 7
    workup.ADDITIONit is treated with a normal sodium hydroxide solution in order
  8. 8
    その他to remove insoluble material
  9. 9
    その他The expected product, which has precipitated
  10. 10
    ろ過is filtered off
  11. 11
    洗浄washed to neutrality
  12. 12
    その他recrystallized from acetic acid

実験手順

0.194 mole (25 g) of 2,5-difluoroaniline is added to 125 ml of pyridine. 0.2 mole (25.5 ml) of benzenesulphonyl chloride is added, while the temperature is between 35° C. and 45° C. The temperature is maintained at 40° C. for 1 hour after the addition is completed, and then the reaction mixture is poured onto 1 kg of ice and water to which 100 ml of concentrated hydrochloric acid have been added. The expected product precipitates. After filtration and washing, it is treated with a normal sodium hydroxide solution in order to remove insoluble material. The soda-containing filtrate is neutralized with concentrated hydrochloric acid. The expected product, which has precipitated, is filtered off, washed to neutrality and recrystallized from acetic acid. It melts at 115° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04725283uspto-grants-1988_02