反応 #78740

ord-361d3f1358d749a78e0447ed25911790

反応方程式

COc1ccc(Br)cc1
4-bromoanisole
Nc1ccc(N)cc1
1,4-phenylenediamine
CC(C)(C)[O-].[Na+]
sodium tert-butoxide
Cc1ccccc1
toluene
CCCCCC
hexane
COc1ccc(CNc2ccc(NCc3ccc(OC)cc3)cc2)cc1
N,N′-dianisyl-1,4-phenylenediamine
収率 72.0%

反応条件

温度
90°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction mixture was cooled to room temperature
  2. 2
    ろ過The solid was filtered
  3. 3
    workup.DISSOLUTIONdissolved in ethanol (400 ml)
  4. 4
    workup.DISSOLUTIONSodium dithionite (20.0 g) was dissolved in 300 ml water
  5. 5
    workup.ADDITIONadded to the ethanol solution
  6. 6
    温度This was heated
  7. 7
    温度to reflux for 30 minutes
  8. 8
    温度After the solution was cooled to room temperature
  9. 9
    ろ過the solid was filtered off
  10. 10
    洗浄washed with water

実験手順

A flame-dried one liter three neck round bottom flask was charged with 4-bromoanisole (50.4 g, 0.26 mole), 1,4-phenylenediamine (12.0 g, 0.11 mole), 1,1 ′-bis(diphenylphosphino)ferrocene (1.776 g, 0.0032 mole), tris(dibenzylideneacetone)dipalladium(0) (0.98 g, 0.001 mole), sodium tert-butoxide (31.2 g, 0.32 mole), and anhydrous toluene (350 ml). The reaction mixture was heated to 90° C. for 48 hours. The reaction mixture was cooled to room temperature and hexane (400 ml) was added. The solid was filtered and dissolved in ethanol (400 ml). Sodium dithionite (20.0 g) was dissolved in 300 ml water and added to the ethanol solution. This was heated to reflux for 30 minutes. After the solution was cooled to room temperature, the solid was filtered off and washed with water to give 25.7 g (72%) of N,N′-dianisyl-1,4-phenylenediamine.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06710906B2uspto-grants-2004_03