反应 #992718

ord-9374108a7280443e8dba6ab2123f1ac4

反应方程式

CC(=O)Nc1ccc2c(c1)Oc1ccc(NC(C)=O)cc1O2
2,7-bis(acetylamino)dibenzodioxin
Ic1ccccc1
iodobenzene
O=C([O-])[O-].[K+].[K+]
potassium carbonate
c1ccc2ncccc2c1
quinoline
O=C(Cc1ccccc1)Nc1ccc2c(c1)Oc1ccc(NC(=O)Cc3ccccc3)cc1O2
crude product
O=C(Cc1ccccc1)Nc1ccc2c(c1)Oc1ccc(NC(=O)Cc3ccccc3)cc1O2
2,7-bis(N-phenylacetylamino)dibenzodioxin

反应条件

温度
170°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度was heated
  2. 2
    温度The reaction mixture was cooled to room temperature
  3. 3
    其他a precipitate was separated by filtration
  4. 4
    workup.ADDITIONTo the filtrate was added 500 ml of water
  5. 5
    其他the organic layer was separated from the aqueous layer
  6. 6
    浓缩The organic layer was concentrated
  7. 7
    其他dried under reduced pressure

实验过程

A slurry prepared from 34.3 g (0.115 mole) of 2,7-bis(acetylamino)dibenzodioxin, 96.4 g (0.576 mole) of iodobenzene, 48.2 g (0.253 mole) of copper (I) iodide, 63.6 g (0.460 mole) of potassium carbonate, and 1500 ml of quinoline was heated with stirring at 170° C. for 48 hours. The reaction mixture was cooled to room temperature, 500 ml of methylene chloride and 500 ml of water were added, and a precipitate was separated by filtration. To the filtrate was added 500 ml of water and the organic layer was separated from the aqueous layer. The organic layer was concentrated and dried under reduced pressure to give 79.4 g of a crude product which was used without purification in the next reaction.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08012606B2uspto-grants-2011_09