反応 #1174484

ord-a6edea3114a84d0bb45b5926bee68136

反応方程式

O=C1c2cccc(Cl)c2C(=O)c2c(Cl)cccc21
1,8-dichloroanthraquinone
NS(=O)(=O)Cc1ccccc1
benzylsulfonamide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Clc1ccccc1
chlorobenzene
O=C1c2cccc(NS(=O)(=O)Cc3ccccc3)c2C(=O)c2c(NS(=O)(=O)Cc3ccccc3)cccc21
1,8-bis(benzylsulfonylamino)anthraquinone

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他A 100ml round bottom flask, equipped with a magnetic stirrer
  2. 2
    温度cooling condenser
  3. 3
    温度This mixture was refluxed for 2.0 hours
  4. 4
    workup.ADDITIONwas added
  5. 5
    その他precipitation
  6. 6
    その他The solid was collected
  7. 7
    抽出extracted with dichloromethane
  8. 8
    workup.ADDITIONtreated with charcoal
  9. 9
    その他recrystallized from a mixture of methanol and dichloromethane
  10. 10
    その他to afford a yellow product

実験手順

A 100ml round bottom flask, equipped with a magnetic stirrer and cooling condenser, was charged with 1,8-dichloroanthraquinone (1.0g), benzylsulfonamide (4.0g), copper acetate monohydrate (1.0g), potassium carbonate (1.4g) and chlorobenzene (20ml). This mixture was refluxed for 2.0 hours and cooled, whereupon methanol (100ml) was added to induce precipitation. The solid was collected, extracted with dichloromethane, treated with charcoal, and recrystallized from a mixture of methanol and dichloromethane to afford a yellow product.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05034547uspto-grants-1991_07