反应 #2358558

ord-47adae46502f4f8782cfec5c646175e4

反应方程式

Cn1c2ccccc2c(=O)c2ccccc21
10-methylacridin-9(10H)-one
O=S(=O)(O)Cl
chlorosulfonic acid
Cn1c2ccc(S(=O)(=O)Cl)cc2c(=O)c2cc(S(=O)(=O)Cl)ccc21
title compound
收率 99.7%
Cn1c2ccc(S(=O)(=O)Cl)cc2c(=O)c2cc(S(=O)(=O)Cl)ccc21
10-methyl-9-oxo-9,10-dihydroacridine-2,7-disulfonyl dichloride
收率 99.7%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度was heated
  2. 2
    温度at reflux for 5 hours
  3. 3
    其他Reaction mixture
  4. 4
    其他condensed
  5. 5
    过滤The yellow precipitate of product was collected by filtration
  6. 6
    洗涤washed with water
  7. 7
    其他dried

实验过程

A mixture of 10-methylacridin-9(10H)-one (4.2 g, 20 mmole) and chlorosulfonic acid (100 mL, 1.5 mole) was heated at reflux for 5 hours. Reaction mixture was then condensed, cooled down to room temperature and poured carefully on 500 g of ice. The yellow precipitate of product was collected by filtration, washed with water and dried to provide 8.1 g of the title compound. This material was used for next step without purification.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09120754B2uspto-grants-2015_09