تفاعل #64834

ord-cdb3f78f85104f2eb3bed0b3a1f986c9

معادلة التفاعل

CCC(C)=O
methylethylketone
c1ccc(Nc2ccccc2)cc1
diphenylamine
CC1(C)c2ccccc2-c2ccccc21
9,9-dimethylfluorene
CC1(C)C2=C(C=CC(N(c3ccccc3)c3ccccc3)C2=O)c2ccccc21
2-(N,N-diphenyl)amino-9,9-dimethylfluorenone
المردود 79.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter the reaction
  2. 2
    درجة الحرارةthe reaction mixture was cooled
  3. 3
    ترشيحsubjected to filtration
  4. 4
    تركيزThe filtrate was concentrated under reduced pressure
  5. 5
    أخرىto obtain a solid
  6. 6
    أخرىto obtain a crystal
  7. 7
    ترشيحThe crystal was recovered by filtration
  8. 8
    أخرىpurified by silica gel column chromatography (eluent: toluene/hexane)

الإجراء التجريبي

16.9 g of diphenylamine, 50.0 g of 9,9-dimethylfluorene, 10.0 g of potassium carbonate anhydride and 3.0 g of copper powder were added to 70 ml of o-dichlorobenze, followed by stirring for 8 hours at 180°-185° C. After the reaction, the reaction mixture was cooled and subjected to filtration. The filtrate was concentrated under reduced pressure to obtain a solid. An appropriate amount of methylethylketone was added to the solid to obtain a crystal. The crystal was recovered by filtration and purified by silica gel column chromatography (eluent: toluene/hexane) to obtain 28.2 g of 2-(N,N-diphenyl)amino-9,9-dimethylfluorenone (Yield: 79%; melting point: 144.2°-145.1° C.).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05415962uspto-grants-1995_05