反応 #350335

ord-1ec54e38ca794699aaba96952205f042

反応方程式

Cl
hydrochloric acid
Cl.Nc1cccc(S(=O)(=O)F)c1
m-Aminobenzenesulfonyl fluoride hydrochloride
Cl
HCl
O=N[O-].[Na+]
Sodium nitrite
O=Cc1cccc(Cl)c1O
3-chloro-2-hydroxy-benzaldehyde
O=Cc1cc(N=Nc2cccc(S(=O)(=O)F)c2)cc(Cl)c1O
3-Chloro-5-(3-fluorosulfonylphenylazo)-2-hydroxy benzaldehyde

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONadded dropwise to the acidic solution
  2. 2
    workup.STIRRINGThe mixture was stirred 30 minutes
  3. 3
    その他The liquid was decanted off
  4. 4
    その他the remaining tarry solid crushed and slurried in 50% HCl
  5. 5
    ろ過The resulting solid was filtered off
  6. 6
    洗浄washed with water and air
  7. 7
    その他dried
  8. 8
    その他the decanted solution yielded an additional 2.8 g

実験手順

m-Aminobenzenesulfonyl fluoride hydrochloride (21.1 g, 0.099 mol) was slurried in hot 10% HCl (300 ml) and then cooled to 0° C. Sodium nitrite (7.0 g, 0.1 mol) was dissolved in 30 ml water and added dropwise to the acidic solution. Vigorous stirring was required to prevent the slurry from coagulating. The diazonium slurry was then added slowly to 500 ml of pyridine containing 3-chloro-2-hydroxy-benzaldehyde (16.0 g, 0.10 mol) at 0° C. The mixture was stirred 30 minutes and then slowly added to 1500 ml ice and hydrochloric acid. The resulting precipitate coagulated into one lump. The liquid was decanted off and the remaining tarry solid crushed and slurried in 50% HCl. The resulting solid was filtered off, washed with water and air dried, (21.1 g). Upon standing 72 hours, the decanted solution yielded an additional 2.8 g. Yield: 23.8 g (70%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04156609uspto-grants-1979_05