反应 #1880945

ord-0c559d4984104c8aaaba634ab0fdd6b6

反应方程式

O=NOS(=O)(=O)O
nitrosylsulfuric acid
[Na+].[OH-]
sodium hydroxide
Cl
hydrochloric acid
Cl
hydrochloric acid
Oc1ccccc1Br
2-bromophenol
N#Cc1ccc(N)cc1
4-cyanoaniline
N#Cc1ccc(N=Nc2ccc(O)c(Br)c2)cc1
4-Hydroxy-3-bromo-4′-cyanoazobenzene

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONare added
  2. 2
    其他is brought to 0° C.
  3. 3
    workup.ADDITIONWhen the addition
  4. 4
    其他to react for a further hour
  5. 5
    过滤the precipitate is filtered off with suction
  6. 6
    洗涤The product is then washed with water
  7. 7
    其他dried

实验过程

18.8 g 4-cyanoaniline are heated at 60° C. in 100 ml water. To dissolve the solid, 10 ml conc. hydrochloric acid are added. A further 115 ml hydrochloric acid are then added, the temperature of the solution is brought to 0° C., 52 g nitrosylsulfuric acid are slowly added dropwise and the mixture is stirred for 1 h. This solution is slowly added dropwise to a solution of 27.5 g 2-bromophenol, 100 ml methanol and 100 ml water at 10° C. A pH of 6–6.5 is maintained by simultaneous addition of 10% sodium hydroxide solution. When the addition is complete, the stirred mass is allowed to react for a further hour and the precipitate is filtered off with suction. The product is then washed with water and dried. The yield of 4-hydroxy-3-bromo-4′-cyanoazobenzene is 68 g.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07022460B2uspto-grants-2006_04