Реакция #2161231

ord-5fda622497ee49eb9ba7276c4ba8b6d3

Уравнение реакции

CC(=O)Nc1ccc2c(c1)CCC2
5-(N-acetylamino)indane
Cc1ccc(I)cc1
p-iodotoluene
O=C([O-])[O-].[K+].[K+]
potassium carbonate
[K+].[OH-]
potassium hydroxide
Cc1ccc(Nc2ccc3c(c2)CCC3)cc1
indan-5-yl-p-tolylamine

Растворители

Условия реакции

Температура
200°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwhile introducing a nitrogen gas
  2. 2
    Другоеhydrolysis at 130° C. for 2 hours
  3. 3
    workup.ADDITIONwas added
  4. 4
    Другоеisoamyl alcohol was removed by azeotropic distillation
  5. 5
    workup.ADDITION200 ml of toluene was added
  6. 6
    workup.DISSOLUTIONto dissolve the reaction product
  7. 7
    ФильтрацияAfter filtration
  8. 8
    ФильтрацияAfter filtering out the magnesium sulfate
  9. 9
    Концентрированиеthe filtrate was concentrated
  10. 10
    Другоеpurified with column chromatography (carrier:silica gel, elute:toluene:hexane=1:4)

Методика

26.28 g (0.15 mol) of 5-(N-acetylamino)indane, 43.61 g (0.20 mol) of p-iodotoluene, 25.88 g (0.188 mol) of anhydrous potassium carbonate and 2.38 g (0.038 mol) of a copper powder were mixed, and while introducing a nitrogen gas, the resulting mixture was heated to 200° C. and stirred for 6 hours. After completion of the reaction, 22.3 g of potassium hydroxide dissolved in 20 ml of water and 50 ml of Isoamyl alcohol were added to conduct hydrolysis at 130° C. for 2 hours. After completion of the hydrolysis 250 ml of water was added, and isoamyl alcohol was removed by azeotropic distillation. 200 ml of toluene was added to dissolve the reaction product. After filtration, the reaction product was dehydrated with magnesium sulfate. After filtering out the magnesium sulfate, the filtrate was concentrated, and purified with column chromatography (carrier:silica gel, elute:toluene:hexane=1:4) to obtain 32.3 of indan-5-yl-p-tolylamine.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07919219B2uspto-grants-2011_04