反应 #586149

ord-dbffa5c681a04933888b3106052a1f12

反应方程式

CSc1cc(-c2cnnn2C(F)(F)F)c(F)cc1Cl
[2-chloro-4-fluoro-5(3-trifluoromethyltriazolyl)phenyl] methyl sulfide
Fc1cc(Cl)c(S)cc1-c1cnnn1C(F)(F)F
2-chloro-4-fluoro-5(3-trifluoromethyltriazolyl)thiophenol
Fc1cc(Cl)ccc1-c1cnnn1C(F)(F)F
2-chloro-4-fluoro-5-(3-trifluoromethyltriazolyl)benzene
收率 85.7%

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

2.2 g (7.1 mmol) of [2-chloro-4-fluoro-5(3-trifluoromethyltriazolyl)phenyl] methyl sulfide was converted to 2-chloro-4-fluoro-5(3-trifluoromethyltriazolyl)thiophenol in the same manner as in Reference Example 1 and then to 1.8 g of 1,1′-thiodi-[2-chloro-4-fluoro-5-(3-trifluoromethyltriazolyl)benzene (yield 85.7%) in the same manner as in Reference Example 5 (1), which was used in Example 2 (4) as the starting material.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07767626B2uspto-grants-2010_08