تفاعل #78740

ord-361d3f1358d749a78e0447ed25911790

معادلة التفاعل

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
المردود 72.0%

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was cooled to room temperature
  2. 2
    ترشيحThe 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
    درجة الحرارةThis was heated
  7. 7
    درجة الحرارةto reflux for 30 minutes
  8. 8
    درجة الحرارةAfter the solution was cooled to room temperature
  9. 9
    ترشيحthe solid was filtered off
  10. 10
    غسيلwashed with water

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06710906B2uspto-grants-2004_03