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
CONDITIONS
反应条件
- 温度
- 50 °C
PROCEDURE
实验过程
To the solution of 2-fluoro-4-(trifluoromethyl)benzoic acid (1 kg, 4.805 mol, 1.00 equivalent “eq.”) and CuCl (14.26 g, 0.144 mol, 0.03 eq.) in t-BuOH (11.7 L) was added triethylamine (TEA, 533.8 g, 5.286 mol, 1.10 eq.) dropwise at room temperature (rt). Then the solution was heated to 50° C. and diphenylphosphoryl azide (DPPA, 1393 g, 5.045 mol, 1.05 eq.) was added dropwise to the solution at 50-60° C. After heating at 80-85° C. overnight the solution was concentrated under vacuum. The residual was dissolved in H2O and filtered. The filtrate was extracted with ethyl acetate. The organic layers was dried with Na2SO4, filtered and concentrated under vacuum. The residual was dissolved in tent-Butyl methyl ether (TBME) and HCl (gas) was bubbled in for 2 hours. The filtrate was collected and dissolved in water and basified with 2 M NaOH. The solution was extracted with TBME. The organic layers were dried and concentrated under vacuum to give 2-fluoro-4-(trifluoromethyl)aniline (498 g, 58%) as a red oil.
WORKUP
后处理
- temperatureAfter heating at 80-85° C. overnight the solution
- concentrationwas concentrated under vacuum
- dissolutionThe residual was dissolved in H2O
- filtrationfiltered
- extractionThe filtrate was extracted with ethyl acetate
- dry with materialThe organic layers was dried with Na2SO4
- filtrationfiltered
- concentrationconcentrated under vacuum
- dissolutionThe residual was dissolved in tent-Butyl methyl ether (TBME) and HCl (gas)
- customwas bubbled in for 2 hours
- customThe filtrate was collected
- dissolutiondissolved in water and basified with 2 M NaOH
- extractionThe solution was extracted with TBME
- customThe organic layers were dried
- concentrationconcentrated under vacuum