反应详情
EQUATION
反应方程式
REACTANTS
反应物
Thionyl chloride
Cl2OS
2,4,5-Trifluorobenzoic acid
C7H3F3O2
Potassium fluoride
FK
3-Chloro-2,4,5-trifluorobenzoic acid
C7H2ClF3O2
3,5-Dichloro-2,4-difluorobenzoyl fluoride
C7HCl2F3O
2,3,4,5-Tetrachlorobenzoyl chloride
C7HCl5O
5-Chloro-2,3,4-trifluorobenzoyl fluoride
C7HClF4O
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The benzoyl halides (1) used as starting materials for this synthetic route are preapred as follows: 3,5-dichloro-2,4-difluorobenzoyl fluoride (boiling point 97°/20 mbar; nD20 =1.5148) and 5-chloro-2,3,4-trifluorobenzoyl fluoride (boiling point 68°-70°/20 mbar; nD20 =1.4764) are obtained together by heating tetrachlorobenzoyl chloride with potassium fluoride in sulpholane at elevated temperatures: ##STR18## The chlorination of 2,4,5-trifluorobenzoic acid in chlorosulphonic acid leads to 3-chloro-2,4,5-trifluorobenzoic acid which is reacted as the crude product with thionyl chloride to give 3-chloro-2,4,5-trifluorobenzoyl chloride (boiling point 94°/18 mbar; nD20 =1.5164): ##STR19##
WORKUP
后处理
- customnD20 =1.4764) are obtained together