تفاعل #2045

ord-c9df1b4f59204cf6ba44f7f63a8372d9

معادلة التفاعل

c1ccc(N(c2ccccc2)c2ccc3c4c(cccc24)CC3)cc1
5-(N,N-diphenylamino)acenaphthene
c1ccc(N(c2ccccc2)c2ccc3c4c(cccc24)CC3)cc1
5-(N,N-diphenylamino)acenaphthene
[Na+].[OH-]
sodium hydroxide
CN(C)C=O
N,N-dimethylformamide
O=P(Cl)(Cl)Cl
phosphorus oxychloride
O=Cc1ccc(N(c2ccccc2)c2ccc3c4c(cccc24)CC3)cc1
5-[N-(4-formylphenyl)-N-phenylamino]acenaphthene
المردود 86.6%

المذيبات

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONThe reaction product was poured into an aqueous solution
  2. 2
    أخرىto precipitate a crystal
  3. 3
    ترشيحthe crystal was filtrated
  4. 4
    غسيلwashed with water
  5. 5
    أخرىdried

الإجراء التجريبي

32.14 g (0.1 mol) of the above prepared 5-(N,N-diphenylamino)acenaphthene was dissolved in 300 ml of N,N-dimethylformamide, and 22.73 g (0.15 mol) of phosphorus oxychloride was dropwise added thereto at room temperature for 30 minutes. After raising the temperature to 50° C., the reaction mixture was stirred for 14 hours. The reaction was determined to be finished when disappearance of 5-(N,N-diphenylamino)acenaphthene was identified. The reaction product was poured into an aqueous solution having 45 g (1.05 mol) of 93% sodium hydroxide dissolved in 1000 ml of water. The resultant mixture was cooled to precipitate a crystal, and the crystal was filtrated, washed with water and dried to obtain 30.27 g (yield: 86.6%, melting point: 138.0°-141.0° C.) of 5-[N-(4-formylphenyl)-N-phenylamino]acenaphthene.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05728500uspto-grants-1998_03