반응 #2161231

ord-5fda622497ee49eb9ba7276c4ba8b6d3

반응 방정식

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

반응 조건

온도
200°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwhile introducing a nitrogen gas
  2. 2
    기타hydrolysis at 130° C. for 2 hours
  3. 3
    workup.ADDITIONwas added
  4. 4
    기타isoamyl 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
    여과After filtration
  8. 8
    여과After filtering out the magnesium sulfate
  9. 9
    농축the filtrate was concentrated
  10. 10
    기타purified with column chromatography (carrier:silica gel, elute:toluene:hexane=1:4)

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07919219B2uspto-grants-2011_04