反応 #816397

ord-25c872cf8d544280ace618887109e235

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONTo this solution was added the reagent solution
  2. 2
    その他prepared above in drops at 5° C. or below
  3. 3
    workup.ADDITIONAfter the dropwise addition
  4. 4
    その他Upon completion of the reaction, extraction
  5. 5
    濃縮was concentrated until dryness under reduced pressure
  6. 6
    workup.DISSOLUTIONThe residue was dissolved in acetone
  7. 7
    workup.ADDITIONby adding 303.2 g of acetone in drops
  8. 8
    workup.ADDITION1600.3 g of water was added in drops at 20° C
  9. 9
    workup.STIRRINGThereafter, the mixture was stirred day and night at 5° C.
  10. 10
    ろ過a solid was recovered by filtration
  11. 11
    その他The solid thus obtained
  12. 12
    洗浄was washed with acetone
  13. 13
    その他dried under reduced pressure

実験手順

Next, 27.1 g (0.10 mole) of dimethyl 4,4′-biphenyldicarboxylate and 133.4 g of THF were introduced to a 2000-ml four-necked reaction vessel. To this solution was added the reagent solution prepared above in drops at 5° C. or below. After the dropwise addition, stirring was continued at 15° C. for 4.5 hours. Upon completion of the reaction, extraction was performed by adding in drops 622.2 g of methylene chloride and 411.2 g of water. The methylene chloride layer obtained was concentrated until dryness under reduced pressure. The residue was dissolved in acetone by adding 303.2 g of acetone in drops and then 1600.3 g of water was added in drops at 20° C. Thereafter, the mixture was stirred day and night at 5° C. and a solid was recovered by filtration. The solid thus obtained was washed with acetone and dried under reduced pressure to give 18.1 g of 4,4′-biphenyldicarboxaldehyde.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07582364B2uspto-grants-2009_09