تفاعل #2049

ord-a22b523213134b988e3fb268968dfa76

معادلة التفاعل

Cc1ccc(Nc2ccc3c4c(cccc24)CC3)cc1
5-[N-(4-tolyl)amino]acenaphthene
Cc1ccc(Nc2ccc3c4c(cccc24)CC3)cc1
5-[N-(4-tolyl)amino]acenaphthene
Ic1ccccc1
iodo benzene
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=[N+]([O-])c1ccccc1
nitrobenzene
Cc1ccc(N(c2ccccc2)c2ccc3c4c(cccc24)CC3)cc1
5-[N-(4-tolyl)-N-phenylamino]acenaphthene
المردود 83.8%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.DISSOLUTIONto dissolve the reaction product
  2. 2
    ترشيحthe mixture was filtrated
  3. 3
    تركيزconcentrated
  4. 4
    أخرىThe concentrated material thus obtained
  5. 5
    أخرىwas purified by column chromatography (carrier: silica gel, eluent: toluene/hexane=1/4)

الإجراء التجريبي

4.66 g (0.018 mol) of the above prepared 5-[N-(4-tolyl)amino]acenaphthene was mixed with 4.99 g (0.022 mol) of iodo benzene, 0.13 g (0.002 mol) of copper powder, 2.76 g (0.02 mol) of anhydrous potassium carbonate and 5 ml of nitrobenzene, and the resultant mixture was stirred at 200° C. for 25 hours. The reaction was determined to be finished when disappearance of 5-[N-(4-tolyl)amino]acenaphthene was identified. 100 ml of toluene was added thereto to dissolve the reaction product, and the mixture was filtrated and concentrated. The concentrated material thus obtained was purified by column chromatography (carrier: silica gel, eluent: toluene/hexane=1/4) to obtain 5.06 g (yield: 83.8%, melting point: 147.0°-148.0° C.) of 5-[N-(4-tolyl)-N-phenylamino]acenaphthene.

المصدر

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