反応 #1687651

ord-693a48ed000e4df3a576a90f19c5a1eb

反応方程式

[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
Cl
HCl
O=C(Cl)c1cc(Cl)ccc1Cl
2,5-dichlorobenzoylchloride
c1ccc(Oc2ccccc2)cc1
phenyl ether
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
O=C(c1ccc(Oc2ccccc2)cc1)c1cc(Cl)ccc1Cl
monomer
収率 73.0%
O=C(c1ccc(Oc2ccccc2)cc1)c1cc(Cl)ccc1Cl
2,5-Dichloro-4'-phenoxybenzophenone
収率 73.0%

反応条件

温度
5°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他To a 22 L open-mouth round bottom flask fitted with a three-necked flange head, a mechanical stirrer, a nitrogen inlet and an outlet
  2. 2
    workup.ADDITIONThe rest was added carefully over about 10 min
  3. 3
    その他was about 35° C.
  4. 4
    workup.ADDITIONafter the addition
  5. 5
    workup.STIRRINGThe mixture was then stirred for about 30 min.
  6. 6
    workup.DISSOLUTIONThe large reddish mass was dissolved
  7. 7
    workup.STIRRINGstirring
  8. 8
    その他The organic layer was separated
  9. 9
    抽出the aqueous layer was extracted with some methylene chloride
  10. 10
    その他After methylene chloride was removed from the combined organic layer by distillation
  11. 11
    その他the residue was recrystallized twice from cyclohexane (2×10 L)
  12. 12
    洗浄washed with cooled hexane, air
  13. 13
    その他dried
  14. 14
    その他vacuum dried

実験手順

To a 22 L open-mouth round bottom flask fitted with a three-necked flange head, a mechanical stirrer, a nitrogen inlet and an outlet connected to an HCl scrubbing tower was added 2,5-dichlorobenzoylchloride (4500 g, 21.5 mol) and phenyl ether (5489 g, 32.3 mol). The solution was cooled in ice to 5° C. under stirring and aluminum chloride (3700 g, 27.8 mol) was added slowly. After about 300 g aluminum chloride was added, the solution started to foam violently. The rest was added carefully over about 10 min. On several occasions, the stirring had to be stopped to control the foaming. The temperature of the reaction mixture was about 35° C. after the addition. The mixture was then stirred for about 30 min. and poured into about 20 gallons of ice water. The large reddish mass was dissolved by adding about 12 L of methylene chloride and stirring. The organic layer was separated and the aqueous layer was extracted with some methylene chloride. After methylene chloride was removed from the combined organic layer by distillation, the residue was recrystallized twice from cyclohexane (2×10 L), washed with cooled hexane, air dried and then vacuum dried to afford 5387 g monomer (73%). The mother liquor was kept for later recovery of remaining product.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05976437uspto-grants-1999_11