HRID399183
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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. 40 Parts of 10% sulfuric acid was added dropwise to hydrolyze the salt, and the reaction mixture was refluxed under for 1 hour. 10 Parts of sodium m-nitrobenzenesulfonate was added, and the mixture was refluxed for 4 hours to give 9.76 parts (98.2% of the theoretical yield) of an unsubstituted quinacridone having an excellent particle diameter as a pigment.
WORKUP
后处理
- stirringthe mixture was stirred at 40° C. for 30 minutes
- customto form a salt
- temperaturethe reaction mixture was refluxed under for 1 hour
- temperaturethe mixture was refluxed for 4 hours
- customto give 9.76 parts (98.2% of the