تفاعل #543545

ord-ae0ec5721e654043af8dd4f1b652492d

معادلة التفاعل

Nc1ccc(-c2ccc(N)c(N)c2)cc1N
3,3′-diaminobenzidine
Cc1ccc(S(=O)(=O)O)cc1.O
p-toluenesulfonic acid monohydrate
CC(C)=N.CC(C)=N.CC(C)=N.CC(C)=N.Nc1ccc(-c2ccc(N)c(N)c2)cc1N
3,3′-diaminobenzidine tetraisopropanimine
المردود 76.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىIn a 200-ml flask equipped with a Soxhlet extractor
  2. 2
    درجة الحرارةby heating
  3. 3
    درجة الحرارةunder reflux in a nitrogen atmosphere for 3 hours
  4. 4
    أخرىacetone was removed under reduced pressure
  5. 5
    workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
  6. 6
    غسيلThe solution was washed with water and 10% aqueous sodium carbonate solution
  7. 7
    أخرىto remove a residual acid component
  8. 8
    أخرىEthyl acetate was removed from the solution under reduced pressure
  9. 9
    أخرىthe residue was purified by silica gel chromatography

الإجراء التجريبي

In a 200-ml flask equipped with a Soxhlet extractor including molecular sieves 4A as a dehydrating agent, a stirrer, a condenser and a thermometer were placed 21.4 g (100 mmol) of 3,3′-diaminobenzidine, 100 ml of acetone and 0.95 g (5 mmol) of p-toluenesulfonic acid monohydrate, followed by heating under reflux in a nitrogen atmosphere for 3 hours. After cooling to room temperature, acetone was removed under reduced pressure, and the residue was dissolved in ethyl acetate. The solution was washed with water and 10% aqueous sodium carbonate solution to remove a residual acid component. Ethyl acetate was removed from the solution under reduced pressure, and the residue was purified by silica gel chromatography to yield 28.5 g (76 mmol) of the target 3,3′-diaminobenzidine tetraisopropanimine [N,N′,N″,N′″-tetraisopropylidene-3,4,3′,4′-biphenyltetramine] in a yield of 76%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07186454B2uspto-grants-2007_03