HRID399181

反应详情

EQUATION

反应方程式

HRID 399181 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

10 Parts of the 6,13-dihydroquinacridone obtained in Example 9 and 80 parts of methanol were charged into a 200-ml flask having a refluxer, and stirred. 12 Parts of a 50% NaOH aqueous solution was added, and the mixture was stirred at 40° C. for 30 minutes to form a salt. 26 Parts of 10% sulfuric acid was added dropwise to hydrolyze the salt, and the reaction mixture was refluxed under heat for 1 hour. 10 Parts of sodium m-nitrobenzenesulfonate was added, and immediately therafter, 3 parts of a 50%. NaOH aqeuous solution was added. Then, the mixture was refluxed for 4 hours to give 9.82 parts (98.8% of the theoretical yield) of an unsubstituted quinacridone having an excellent particle diameter as a pigment.

WORKUP

后处理

  1. stirringthe mixture was stirred at 40° C. for 30 minutes
  2. customto form a salt
  3. temperaturethe reaction mixture was refluxed
  4. temperatureunder heat for 1 hour
  5. temperatureThen, the mixture was refluxed for 4 hours
  6. customto give 9.82 parts (98.8% of the