Method for the production of disubstituted imidazolium salts
Process for preparing 1,3-disubstituted imidazolium salts of the formula I where R1 and R3 are each, independently of one another, an organic radical having from 1 to 20 carbon atoms, R2, R4 and R5 are each, independently of one another, an H atom or an organic radical having from 1 to 20 carbon atoms, X is the anion of a hydrogen acid having a pK a of at least 2 (measured at 25° C., 1 bar in water or dimethyl sulfoxide) and n is 1, 2 or 3, wherein a) an α-dicarbonyl compound, an aldehyde, an amine and the hydrogen acid of the anion X − are reacted with one another and b) the reaction is carried out in water, a solvent which is miscible with water or a mixture thereof.
1. A process for preparing a 1,3-disubstituted imidazolium salt represented by the following formula I:
wherein
each of R1 and R3 is, independently of one another, a C1-C10-alkyl group,
each of R2, R4 and R5 is, independently of one another, an H atom or a C1-C10-alkyl group,
X is the anion of a hydrogen acid having a pK a of at least 2, measured at 25° C., 1 bar in water or dimethyl sulfoxide, and
n is 1, 2 or 3,
the process comprising:
reacting an α-dicarbonyl compound, an aldehyde, an amine and the hydrogen acid of the anion X − with one another in a single stage, thereby obtaining a reaction product,
wherein the reacting is carried out in water, a solvent which is miscible with water or a mixture thereof, and the solubility of the imidazolium salt is at least 50 grams per 1 liter of water at 1 bar and 21° C.,
wherein X is selected from the group consisting of a benzoate anion, an anion of a C1-C20 alkanecarboxylic acid, and a mixture thereof,
wherein the reaction mixture does not comprise a hydrophobic organic solvent which is immiscible with water, and wherein removal of said water or solvent after the reaction is carried out without using a hydrophobic organic solvent which is immiscible with water.
2. The process according to claim 1 , wherein R1 and R3 are the same and the imidazolium salt is a symmetrical, disubstituted imidazolium salt.
3. The process according to claim 1 , wherein the imidazolium salt is a mixture of imidazolium salts of the formula I.
4. The process according to claim 1 , wherein n is 1.
5. The process according to claim 1 , wherein the pK a of the hydrogen acid of the anion X is from 3 to 8.
6. A process for preparing a 1,3-disubstituted imidazolium salt represented by the following formula I:
wherein
each of R1 and R3 is, independently of one another, a C1-C10-alkyl group,
each of R2, R4 and R5 is, independently of one another, an H atom or a C1-C10-alkyl group,
X is the anion of a hydrogen acid having a pK a of at least 2, measured at 25° C., 1 bar in water or dimethyl sulfoxide, and
n is 1, 2 or 3,
the process comprising:
reacting an α-dicarbonyl compound, an aldehyde, an amine and the hydrogen acid of the anion X − with one another in a single stage, thereby obtaining a reaction product,
wherein the reacting is carried out in water, a solvent which is miscible with water or a mixture thereof, and the solubility of the imidazolium salt is at least 50 grams per 1 liter of water at 1 bar and 21° C.,
wherein X is the anion of a compound having at least one carboxylate group.
7. The process according to claim 6 , wherein X is the acetate anion.
8. The process according to claim 1 , wherein the α-dicarbonyl compound is a compound represented by the following formula II
R4-CO—CO—R5 II,
wherein R4 and R5 are as defined in claim 1 .
9. The process according to claim 8 , wherein the α-dicarbonyl compound is glyoxal.
10. The process according to claim 1 , wherein the aldehyde is an aldehyde of the formula R2-CHO, where R2 is as defined in claim 1 .
11. The process according to claim 1 , wherein the amine is an amine of the formula R1-NH2 or a mixture of amines having different radicals R1.
12. The process according to claim 1 , wherein the hydrogen acid of the anion X is a C1-C20 alkanecarboxylic acid.
13. The process according to claim 1 , wherein the hydrogen acid of the anion X is acetic acid.
14. The process according to claim 1 , wherein the reaction is carried out in water.
15. The process according to claim 1 , wherein the water or the water-comprising solvent mixture is distilled off without use of an entrainer after the reaction.
16. The process according to claim 1 , wherein the process is carried out continuously.
17. The process according to claim 1 which is carried out continuously and in which the α-dicarbonyl compound, the aldehyde and, optionally, the hydrogen acid of the anion X, are mixed beforehand and fed together as one feed stream into the reaction vessel.
18. The process according to claim 1 , wherein the reaction product obtained is treated with an oxidant.
19. The process according to claim 18 , wherein the oxidant is hydrogen peroxide.
20. A process for preparing a 1,3-disubstituted imidazolium salt represented by the following formula I:
wherein
each of R1 and R3 is, independently of one another, an organic radical having from 1 to 20 carbon atoms,
each of R2, R4 and R5 is, independently of one another, an H atom or an organic radical having from 1 to 20 carbon atoms,
X is the anion of a hydrogen acid having a pK a of at least 2, measured at 25° C., 1 bar in water or dimethyl sulfoxide, and
n is 1, 2 or 3,
the process comprising:
reacting an α-dicarbonyl compound, an aldehyde, an amine, and the hydrogen acid of the anion X − in a reaction mixture with one another in a single stage, thereby obtaining a reaction product,
wherein the reacting is carried out in water, a solvent which is miscible with water or a mixture thereof, with the proviso that the reaction mixture does not comprise a hydrophobic organic solvent which is immiscible with water during and/or after the reaction.
21. The process of claim 1 , which is a continuous process.
22. The process of claim 6 , which is a continuous process.
23. The process of claim 20 , which is a continuous process.
24. The process of claim 6 , wherein the reaction mixture does not comprise a hydrophobic organic solvent which is immiscible with water, and wherein removal of said water or solvent after the reaction is carried out without using a hydrophobic organic solvent which is immiscible with water.
25. The process of claim 20 , wherein removal of said water or solvent after the reaction is carried out without using a hydrophobic organic solvent which is immiscible with water.