Réaction #727844
ord-2f047d25789c41b9a45450a8db5118ab
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1workup.DISTILLATIONazeotrope are distilled off at atmospheric pressure (85-101° C.)
- 2workup.ADDITIONAfter four further azeotropic distillations with 100 ml of 1,4-dioxane each time, a further 19 g of approx. 80% aqueous trifluoroacetic acid are added to the residue
- 3workup.ADDITION100 ml of 1,4-dioxane are subsequently added
- 4workup.ADDITION105 ml of HCl- and CF3C(O)OH-containing water/dioxane
- 5workup.DISTILLATIONazeotrope are distilled off at atmospheric pressure
- 6SéchageAfter three further azeotropic distillations with 100 ml of 1,4-dioxane each time and drying of the distillation residue under reduced pressure at 1.3 Pa and 70° C.
Mode opératoire
Analogously to Example 1, 23.0 g (0.132 mol) of 1-butyl-3-methylimidazolium chloride are reacted with 28.0 g of approx. 80% aqueous trifluoroacetic acid, CF3C(O)OH (50% excess). 100 ml of 1,4-dioxane are subsequently added, and 112 ml of HCl- and CF3C(O)OH-containing water/dioxane azeotrope are distilled off at atmospheric pressure (85-101° C.). After four further azeotropic distillations with 100 ml of 1,4-dioxane each time, a further 19 g of approx. 80% aqueous trifluoroacetic acid are added to the residue. 100 ml of 1,4-dioxane are subsequently added, and 105 ml of HCl- and CF3C(O)OH-containing water/dioxane azeotrope are distilled off at atmospheric pressure. After three further azeotropic distillations with 100 ml of 1,4-dioxane each time and drying of the distillation residue under reduced pressure at 1.3 Pa and 70° C., 1-butyl-3-methylimidazolium trifluoroacetate is obtained. The yield is approximately quantitative.