반응 #216028

ord-d84f2bc38f31467d826cb0dc0d432224

반응 방정식

O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=C(c1ccc(F)cc1)c1ccc(F)cc1
4,4'-difluorobenzophenone
Oc1ccc(-c2ccc(O)cc2)cc1
4,4'-dihydroxybiphenyl
N#Cc1ccc([N+](=O)[O-])cc1C#N
4-nitrophthalonitrile
N#Cc1ccccc1C#N
phthalonitrile

반응 조건

온도
160°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타To a 100 ml, 3-necked flask equipped with a thermometer
  2. 2
    workup.ADDITIONwas added
  3. 3
    workup.STIRRINGThe reaction content was stirred at 90° C. for 1 hour
  4. 4
    온도The reaction mixture was refluxed at 145°-150° C. for 10 hours
  5. 5
    기타was removed by azeotropic distillation
  6. 6
    기타The toluene was removed by distillation
  7. 7
    workup.ADDITIONwas added
  8. 8
    workup.STIRRINGThe reaction content was then stirred at the ambient temperature for 2 hours and at 90° C. for 6 hours
  9. 9
    workup.STIRRINGwith stirring
  10. 10
    여과The solid precipitate was collected by suction filtration
  11. 11
    세척washed exhaustively with water
  12. 12
    기타dried

실험 절차

To a 100 ml, 3-necked flask equipped with a thermometer and a Dean-Stark trap was added 3.52 gm (16.1 mmol) of 4,4'-difluorobenzophenone, 4.0 gm (21.5 mmol) of 4,4'-dihydroxybiphenyl, and 40 ml of dimethylacetamide (DMAC). After flushing the mixture for 30 minutes with dry nitrogen, 5.0 gm (36.2 mmol) of pulverized anhydrous potassium carbonate was added with stirring. The reaction content was stirred at 90° C. for 1 hour. Toluene was added to the Dean-Stark trap and to the reaction vessel (4 ml). The reaction mixture was refluxed at 145°-150° C. for 10 hours. Water which formed as a by-product was removed by azeotropic distillation. The toluene was removed by distillation while heating to 160° C. Upon cooling to ambient condition, 1.86 gm (10.7 mmol) of 4-nitrophthalonitrile was added. The reaction mixture turned purple. The reaction content was then stirred at the ambient temperature for 2 hours and at 90° C. for 6 hours. The reaction was monitored by FTIR spectroscopy and showed the complete disappearance of the absorptions attributed to the nitro and hydroxyl groups. The room temperature mixture was poured into 200 ml of water with stirring. The solid precipitate was collected by suction filtration, washed exhaustively with water, and dried to afford 7.8 gm of oligomeric phthalonitrile monomer.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05464926uspto-grants-1995_11