Ammonium salt having saccharin anion

Abstract

An ammonium salt having a saccharin anion, which is represented by formula (1), exhibits excellent thermal stability even though no halogen atom is contained therein. ##STR00001##
(In the formula, each of R.sup.1-R.sup.4 independently represents an alkyl group having 1-4 carbon atoms or an alkoxyalkyl group that is represented by —(CH.sub.2).sub.n—OR (wherein R represents an alkyl group having 1-4 carbon atoms, and n represents an integer of 1 or 2). Incidentally, any two of the R.sup.1-R.sup.4 may combine with each other to form a ring together with a nitrogen atom.

Claims

1. An ammonium salt having a saccharin anion, represented by formula (1): ##STR00011## wherein any one of the R.sup.1 to R.sup.4 is an alkoxyalkyl group of —(CH.sub.2).sub.n—OR wherein R is an alkyl group having 1 to 4 carbon atoms and n is an integer of 1 or 2, remaining three of the R.sup.1 to R.sup.4 are each independently an alkyl group having 1 to 4 carbon atoms, provided that any two of the remaining three of the R.sup.1 to R.sup.4 may combine with each other to form a ring together with the nitrogen atom.

2. The ammonium salt of claim 1, being an ionic liquid having a melting point of 25° C. or less.

3. The ammonium salt of claim 1, having the formula (2): ##STR00012## wherein Me is a methyl group, and Et is an ethyl group.

4. The ammonium salt of claim 1, having the formula (3): ##STR00013## wherein Me is a methyl group.

5. The ammonium salt of claim 1, having the formula (4): ##STR00014## wherein Me is a methyl group.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a .sup.1H-NMR spectrum of a compound [1] obtained in Example 1.

(2) FIG. 2 is a differential scanning calorimetry (DSC) chart of the compound [1] obtained in Example 1.

(3) FIG. 3 is a thermogravimetry-differential thermal analysis (TG-DTA) chart of the compound [1] obtained in Example 1.

(4) FIG. 4 is a .sup.1H-NMR spectrum of a compound [2] obtained in Example 2.

(5) FIG. 5 is a DSC chart of the compound [2] obtained in Example 2.

(6) FIG. 6 is a TG-DTA chart of the compound [2] obtained in Example 2.

(7) FIG. 7 is a .sup.1H-NMR spectrum of a compound [3] obtained in Example 3.

(8) FIG. 8 is a DSC chart of the compound [3] obtained in Example 3.

(9) FIG. 9 is a TG-DTA chart of the compound [3] obtained in Example 3.

DESCRIPTION OF EMBODIMENTS

(10) Hereinafter, the invention is described in more detail.

(11) The ammonium salt having a saccharin anion of the invention is represented by the formula (1).

(12) ##STR00006##

(13) In the formula (1), R.sup.1 to R.sup.4 are each independently an alkyl group having 1 to 4 carbon atoms or an alkoxyalkyl group of —(CH.sub.2).sub.n—OR wherein R is an alkyl group having 1 to 4 carbon atoms and n is an integer of 1 or 2, provided that any two of the R.sup.1 to R.sup.4 may combine with each other to form a ring together with a nitrogen atom.

(14) The R.sup.1 to R.sup.4 and R may be a linear, branched, or cyclic alkyl group having 1 to 4 carbon atoms, and specific examples of the alkyl group include methyl, ethyl, n-propyl, i-propyl, c-propyl, n-butyl, i-butyl, s-butyl, t-butyl, and c-butyl groups. Among the groups, the alkyl groups having 1 to 3 carbon atoms are preferable, and the methyl and ethyl groups are more preferable.

(15) Examples of the ring structure in which any two of the R.sup.1 to R.sup.4 combine with each other to form the ring together with the nitrogen atom include aziridine, azetidine, pyrrolidine, and piperidine rings, and among the rings, the pyrrolidine ring is preferable.

(16) In particular, from the viewpoint that the ammonium salt is likely to be liquid as an ionic liquid at room temperature (25° C.), the ammonium salt of the invention preferably has, as any one of the R.sup.1 to R.sup.4, an alkoxyalkyl group of —(CH.sub.2).sub.n—OR in which R is preferably an alkoxyalkyl group having 1 to 3 carbon atoms. The remaining three of the R.sup.1 to R.sup.4 preferably each independently have a cation structure that is alkyl group having 1 to 4, preferably 1 to 3 carbon atoms (provided that any two of the alkyl groups may combine with each other to form a ring together with the nitrogen atom), and more preferably each independently have any of the cation structures of the following formulae.

(17) ##STR00007##
(In the formulae, Me is a methyl group, and Et is an ethyl group.)

(18) The ammonium salt of the invention can be obtained through, for example, mixing a predetermined quaternary ammonium salt halide produced in accordance with a conventional method (such as a chloride or a bromide) and a commercially available saccharin metal salt (such as a sodium salt) in an organic solvent capable of dissolving the halide and the salt even partially (such as acetonitrile) for base exchange. In many cases, the saccharin salt produced as the desired product is dissolved in the solvent, and the inorganic salt as a by-product (such as a sodium chloride salt) is precipitated as a solid. Therefore, the desired product can be obtained through filtering the solution as it is and concentrating the solvent. If necessary, a high-purity product can be obtained through treating the predetermined quaternary ammonium salt halide with an OH-type strongly basic anion exchange resin for ion exchange of the halide ion with a hydroxide ion to obtain a quaternary ammonium salt hydroxide, and neutralizing the quaternary ammonium salt hydroxide with saccharin in an aqueous solvent.

(19) After completion of the reaction, water is removed to obtain the desired product.

EXAMPLES

(20) Examples are given below for further illustrating the invention although the invention is not limited thereto.

(21) The analyzers and the conditions used in Examples are as follows.

(22) [1] spectrum

(23) Device: JNM-ECZ400S manufactured by JEOL Ltd.

(24) Solvent: Deuterated chloroform

(25) [2] DSC

(26) Device: DSC 6200 manufactured by Seiko Instruments Inc.

(27) Measurement condition: Measurement was performed under the condition that the temperature was raised at a rate of 10° C. per minute from 25° C. to 40° C., lowered at a rate of 1° C. per minute from 40° C. to −70° C., held at −70° C. for 1 minute, and then raised at a rate of 1° C. per minute from −70° C. to 40° C.
[3] TG-DTA

(28) Device: TG-DTA 6200 manufactured by Seiko Instruments Inc. ([Examples 2 and 3]) Thermo Plus TG8120 manufactured by Rigaku Corporation ([Example 1])

(29) Measurement condition: Measurement was performed under the condition that the temperature was raised at a rate of 10° C. per minute from 20° C. to 500° C. in an air atmosphere.

[Example 1] Synthesis of Compound [1]

(30) ##STR00008##
(In the formula, Me is a methyl group.)

(31) Pyrrolidine (1.51 parts by weight) (manufactured by FUJIFILM Wako Pure Chemical Corporation) and 2-methoxyethyl chloride (1.00 part by weight) (manufactured by KANTO CHEMICAL CO., INC.) were mixed and reacted for 1 hour while refluxed. Through the reaction, the reaction solution was separated into two layers, and then allowed to cool for a while to solidify the lower layer. Only the upper layer was collected through decantation and purified through vacuum distillation to obtain 0.96 parts by weight of N-2-methoxyethylpyrrolidine (boiling point 76° C./vapor pressure 45 mmHg) as a desired product (yield 70%).

(32) To 1.00 part by weight of the obtained N-2-methoxyethylpyrrolidine, tetrahydrofuran (THE) was added at 10 times the volume of the N-2-methoxyethylpyrrolidine, the resulting mixture was cooled in an ice bath, and 1.22 parts by weight of methyl iodide (manufactured by FUJIFILM Wako Pure Chemical Corporation) was added. After a while, a white solid was precipitated. After 30 minutes, the ice bath was removed, and the mixture was stirred at room temperature overnight. Then, the reaction solution was filtered wider reduced pressure to collect the precipitated white solid, and the white solid was recrystallized in an acetonitrile-tetrahydrofuran mixed solvent system to obtain 1.71 parts by weight of N-2-methoxyethyl-N-methylpyrrolidinium iodide (yield 81%).

(33) To 1.00 part by weight of the obtained N-2-methoxyethyl-N-methylpyrrolidinium iodide, 2.00 parts by weight of ion-exchanged water was added, and the N-2-methoxyethyl-N-methylpyrrolidinium iodide was dissolved. Separately, a strongly basic ion exchange resin, ORLITE DS-2 (manufactured by ORGANO CORPORATION, exchange capacity 1.4 meq/ml, OH-type) was thoroughly washed so that the cleaning solution used for washing was neutral, and the ion exchange resin equivalent to 2.5 times the molar amount of the N-2-methoxyethyl-N-methylpyrrolidinium iodide was put into a plastic container and added to the N-2-methoxyethyl-N-methylpyrrolidinium iodide. After 6 to 7 hours, the ion exchange resin was filtered off with a Kiriyama funnel. To the filtrate, washed ORLITE DS-2 equivalent to 2.5 times the molar amount of the raw material was newly added and left overnight, and then the ion exchange resin was filtered off with a Kiriyama funnel to obtain a solution in which most of the salt was converted from the chloride salt to a hydroxide. Furthermore, the filtrate was flowed through a column packed with ORLITE DS-2 (equivalent to 5 times the molar amount of the raw material) at a space velocity SV=1 for treatment to obtain a hydroxide aqueous solution for a neutralization reaction.

(34) To the hydroxide aqueous solution, 0.61 parts by weight of saccharin (also known as o-sulfobenzimide, manufactured by Tokyo Chemical Industry Co., Ltd.) was added, and the resulting mixture was stirred to dissolve the saccharin. Then, saccharin was added little by little while the pH was checked with a pH test paper, and the mixing was completed when the pH test paper showed a pH of 7. From the aqueous solution, most of the water was removed with an evaporator, and then the resulting product was put under vacuum using a vacuum pump at 45° C. (using an oil bath) for 3 hours or more to obtain a desired product, 1.11 parts by weight of N-2-methoxyethyl-N-methylpyrrolidinium saccharinate (compound [1]) as a colorless transparent liquid (25° C.) (yield 92%). FIG. 1 shows the .sup.1H-NMR chart (solvent: deuterated chloroform), FIG. 2 shows the DSC chart, and FIG. 3 shows the TG-DTA chart.

[Example 2] Synthesis of Compound [2]

(35) ##STR00009##
(In the formula, Me is a methyl group, and Et is an ethyl group.)

(36) Diethylamine (1.00 part by weight) (manufactured by KANTO CHEMICAL CO., INC.) and 2-methoxyethyl chloride (1.24 parts by weight) (manufactured by KANTO CHEMICAL CO., INC.) were mixed, and the resulting mixed solution was put in an autoclave and reacted at 100° C. for 24 hours. At this time, the internal pressure was 1.3 kgf/cm.sup.2. After 24 hours, to the mixture of a precipitated crystal and the reaction solution, an aqueous solution was added in which 0.79 parts by weight of potassium hydroxide (manufactured by KATAYAMA CHEMICAL INDUSTRIES Co., Ltd.) was dissolved in 2.00 parts by weight of water to obtain two organic layers, and the two organic layers were separated with a separatory funnel. Furthermore, an operation was performed twice in which 1.87 parts by weight of methylene chloride (manufactured by FUJIFILM Wako Pure Chemical Corporation) was added and extraction was performed. The separated organic layers were put together, washed with saturated brine, potassium carbonate (manufactured by FUJIFILM Wako Pure Chemical Corporation) was added, and the resulting mixture was dried and filtered under reduced pressure. The solvent of the obtained organic layer was removed using a rotary evaporator, the residue was distilled at atmospheric pressure, and a fraction having a boiling point of around 135° C. was obtained to obtain 0.26 parts by weight of N,N-diethyl-N-2-methoxyethylamine as a desired product (yield 30%).

(37) As a colorless transparent liquid (25° C.), 1.12 parts by weight of N,N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium saccharinate (compound [2]) was obtained in the same manner as in Example 1 except that the N,N-diethyl-N-2-methoxyethylamine obtained above was used in place of N-2-methoxyethylpyrrolidine (yield 93%). FIG. 4 shows the .sup.1H-NMR chart (solvent: deuterated chloroform), FIG. 5 shows the DSC chart, and FIG. 6 shows the TG-DTA chart.

[Example 3] Synthesis of Compound [3]

(38) ##STR00010##
(In the formula, Me is a methyl group.)

(39) To 22.2 parts by weight of 1-methylpyrrolidine (manufactured by FUJIFILM Wako Pure Chemical Corporation), tetrahydrofuran (THF) was added at 10 times the volume of the 1-methylpyrrolidine, and while the resulting mixture was cooled with ice and stirred, 21.1 parts by weight of chloromethyl methyl ether (manufactured by Tokyo Chemical Industry Co., Ltd.) was added. Although a crystal was immediately precipitated, the mixture was kept to be stirred overnight. Then, the reaction solution was filtered under reduced pressure to collect the precipitated solid, the solid was dried under reduced pressure using a vacuum pump to obtain 38.2 parts by weight of N-methoxymethyl-N-methylpyrrolidinium chloride as a white solid (yield 89%).

(40) To 15.7 parts by weight of saccharin sodium dihydrate (manufactured by Tokyo Chemical Industry Co., Ltd.), methanol was added at 10 times the volume of the saccharin sodium dihydrate, and the resulting mixture was stirred to dissolve the saccharin sodium dihydrate. To the resulting solution, a solution was added in which 10.8 parts by weight of the N-methoxymethyl-N-methylpyrrolidinium chloride synthesized above was dissolved in methanol having a volume of 15 times of the N-methoxymethyl-N-methylpyrrolidinium chloride, and the resulting mixture was reacted overnight at room temperature.

(41) The reaction solution was concentrated, put under vacuum, and then dissolved in a minimized amount of acetonitrile. The resulting solution was added to a large amount of toluene, and a precipitated solid was filtered off. The filtrate was concentrated, the above-described operation was performed once again, and then the filtrate was concentrated and dried under reduced pressure using a vacuum pump to obtain a desired product, 18.9 parts by weight of N-methoxymethyl-N-methylpyrrolidinium saccharinate (compound [3]) as a colorless transparent liquid (25° C.) (yield 93%). FIG. 7 shows the .sup.1H-NMR chart (solvent: deuterated chloroform), FIG. 8 shows the DSC chart, and FIG. 9 shows the TG-DTA chart.