JP2006206456A - New amide salt and its utilization - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an amide salt having an anion with a prescribed structure. <P>SOLUTION: The invention provides an amide salt represented by formula (1) (wherein Rf<SP>1</SP>is a group in which all hydrogen atoms of monovalent organic group having an alkyl chain containing an ether bond in at least a part of the chemical structure is substituted with fluorine atoms; Rf<SP>2</SP>is a group in which all hydrogen atoms of monovalent organic group containing or not containing an ether bond are substituted with fluorine atoms; Y+ is a cation other than a hydrogen ion). <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention relates to a salt (amide salt) having an anion having a structure in which a sulfonyl group and a carbonyl group are bonded to a nitrogen atom. The present invention also relates to a method for producing such an amide salt. Such an amide salt can be used, for example, as an electrolyte for various power storage elements.

Liquid salt exhibiting (. Hereinafter, also referred to as "room temperature molten salt") in the normal temperature range as the anion, which may constitute, bis (trifluoromethanesulfonyl) imide anion ^{_{[- N (SO 2 CF 3}} ) 2, hereinafter "TFSI" both Say. ]It has been known. A typical example of a room temperature molten salt having such an anion is a salt of 1-ethyl-3-methylimidazolium cation (EMI) and TFSI.
Patent Document 1 below describes an onium salt having an amide anion having a structure in which a sulfonyl group and a carbonyl group are bonded to a nitrogen atom. Examples of such amide anion, 2,2,2-trifluoro -N- (trifluoromethanesulfonyl) acetamide anion _{^{[- N (COCF 3) (}} SO 2 CF 3)] have been described. This is an anion corresponding to a chemical structure in which one of two trifluoromethanesulfonyl groups (SO ₂ CF ₃ ) contained in TFSI is changed to a trifluoromethanecarbonyl group (COCF ₃ ). Such an onium salt of an asymmetric amide anion is considered to have a lower melting point than the corresponding salt of a symmetric anion. Other prior art documents relating to a salt having an anion having a structure in which a sulfonyl group and a carbonyl group are bonded to a nitrogen atom include Patent Documents 2 and 3 below.
JP 2003-201272 A JP 2002-75443 A International Publication No. 03/012900 Pamphlet

Here, regarding a salt of a type having an anion having a structure in which a sulfonyl group (—SO ₂ —) and a carbonyl group (—CO—) are bonded to a nitrogen atom, the characteristics (for example, electrochemical stability, ionic conductivity) It is beneficial if one or more of the properties of low melting point, low viscosity, etc. can be improved.
An object of the present invention is to provide a novel salt (amide salt) having an anion having a structure in which a sulfonyl group and a carbonyl group are bonded to a nitrogen atom. Another object of the present invention is to provide a process for producing such amide salts. Another object of the present invention is to provide a novel amide suitable as a raw material (intermediate) for producing such an amide salt and a method for producing the same. Still another object of the present invention is to provide an electrolyte containing the amide salt and a storage element (battery, capacitor, etc.) provided with the electrolyte.

According to the present invention, an amide salt represented by the following formula (1) is provided.

Rf ¹ in the above formula (1) represents all hydrogen atoms of a monovalent organic group (typically a hydrocarbon group) having an alkyl chain containing an ether bond in at least a part of its chemical structure as fluorine atoms. It is a group that has been replaced. In the present specification, a group in which all hydrogen atoms of any organic group are replaced with fluorine atoms may be represented by adding “perfluoro” to the name of the organic group. For example, with respect to an “alkyl group”, a group in which all of its hydrogen atoms are replaced with fluorine atoms may be referred to as a “perfluoroalkyl group”. In addition, such a group in which all hydrogen atoms of an organic group are replaced with fluorine atoms may be collectively referred to as a “perfluoro group”. Similarly, a structure portion in which all hydrogen atoms in an alkyl chain are replaced with fluorine atoms may be referred to as a “perfluoroalkyl chain”. Therefore, Rf ¹ in the above formula (1) may be a perfluoro group having a perfluoroalkyl chain containing an ether bond in at least a part of its chemical structure (this is referred to as “perfluoroalkyl ether chain”). .
A typical example of Rf ^{1 in} the amide salt disclosed herein includes a perfluoroalkyl group containing an ether bond. For example, a group (CF ₃ OCF ₂ —) in which all hydrogen atoms of a methoxymethyl group are replaced with fluorine atoms is an example of a perfluoroalkyl group containing an ether bond (this is referred to as “perfluoroalkyl ether group”). is there.
Rf ² in the above formula (1) is a group in which all hydrogen atoms of a monovalent organic group (typically a hydrocarbon group) are replaced with fluorine atoms (ie, a perfluoro group). This Rf ² may be a perfluoro group containing an ether bond. Rf ² may be a perfluoro group containing no ether bond. A typical example of Rf ^{2 in} the amide salt disclosed herein includes a group in which all hydrogen atoms of an alkyl group not containing an ether bond are replaced with fluorine atoms (that is, a perfluoroalkyl group).

Y ⁺ in the above formula (1) is a monovalent cation other than hydrogen ions. This Y ⁺ can be an inorganic cation. For example, it may be an alkali metal cation such as lithium (Li), sodium (Na), or potassium (K).

The cation (Y ⁺ ) may be an organic cation. For example, a monovalent organic cation containing at least one element selected from nitrogen (N), sulfur (S), oxygen (O), and phosphorus (P) (referred to as a cation of an organic compound; the same shall apply hereinafter). possible. Further, it may be an organic cation composed of at least one element other than those described above and having a lone electron pair in a neutral state.
Y ⁺ in the present invention each has an imidazolium ion (which refers to a cation having an imidazole skeleton; the same shall apply hereinafter), thiazolium ion, oxazolium ion, isoxazolium ion, triazolium ion, which may have a substituent. It can be any cation selected from the group consisting of pyridinium ion, pyridazinium ion, pyrimidinium ion, pyrazinium ion, ammonium ion, phosphonium ion and sulfonium ion. For example, it may be any organic cation represented by the following formulas (3) to (7) and (9).

ここで、上記式（３）中のＲ¹¹〜Ｒ¹⁵は、それぞれ独立に、水素原子、ハロゲン原子および炭素数１〜１０の有機基から選択され得る。Ｒ¹¹〜Ｒ¹⁵のうち二つ以上が相互に結合して環構造を形成していてもよい。 That is, Y ⁺ can be an organic cation represented by the following formula (3).

Here, R ^{11 to} R ¹⁵ in the above formula (3) can be independently selected from a hydrogen atom, a halogen atom and an organic group having 1 to 10 carbon atoms. Two or more of R ^{11 to} R ¹⁵ may be bonded to each other to form a ring structure.

In one preferred embodiment of the cation represented by the above formula (3), R ^{11 to} R ¹⁵ in the formula (3) are each independently a hydrogen atom and a C 1-10 substitution (eg, halogen substitution). Or it may be selected from unsubstituted alkyl groups. In another preferred embodiment, among R ^{11 to} R ¹⁵ in the formula (3), R ¹¹ and R ¹³ are each independently selected from alkyl groups having 1 to 4 carbon atoms, and the other (ie, R ¹² , R ¹⁴ and R ¹⁵ ) may each independently be selected from a hydrogen atom and an alkyl group having 1 to 4 carbon atoms. For example, each of R ^{11 to} R ¹³ may be independently selected from an alkyl group having 1 to 4 carbon atoms, and the other may be a cation having a structure selected from a hydrogen atom and an alkyl group having 1 to 4 carbon atoms. R ^{11 to} R ¹⁴ may be independently selected from an alkyl group having 1 to 4 carbon atoms, and R ¹⁵ may be a cation having a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. Further, all of R ^{11 to} R ¹⁵ may be cations independently selected from alkyl groups having 1 to 4 carbon atoms.

ここで、上記式（４）中のＲ²¹〜Ｒ²⁶は、それぞれ独立に、水素原子、ハロゲン原子および炭素数１〜１０の有機基から選択され得る。Ｒ²¹〜Ｒ²⁶のうち二つ以上が相互に結合して環構造を形成していてもよい。 Y ⁺ may be an organic cation represented by the following formula (4).

Here, R ^{21 to} R ²⁶ in the above formula (4) can be independently selected from a hydrogen atom, a halogen atom and an organic group having 1 to 10 carbon atoms. Two or more of R ^{21 to} R ²⁶ may be bonded to each other to form a ring structure.

ここで、上記式（５）中のＲ³¹〜Ｒ³⁴は、それぞれ独立に、水素原子、ハロゲン原子および炭素数１〜１０の有機基から選択され得る。Ｒ³¹〜Ｒ³⁴のうち二つ以上が相互に結合して環構造を形成していてもよい。 Y ⁺ may be an organic cation represented by the following formula (5).

Here, R ^{31 to} R ³⁴ in the above formula (5) can be independently selected from a hydrogen atom, a halogen atom, and an organic group having 1 to 10 carbon atoms. Two or more of R ^{31 to} R ³⁴ may be bonded to each other to form a ring structure.

ここで、上記式（６）中のＲ⁴¹〜Ｒ⁴⁴は、それぞれ独立に、水素原子および炭素数１〜１０の有機基から選択され得る。Ｒ⁴¹〜Ｒ⁴⁴のうち二つ以上が相互に結合して非芳香族性の環を形成していてもよい。 Y ⁺ may be an organic cation represented by the following formula (6).

Here, R ^{41 to} R ⁴⁴ in the above formula (6) can be independently selected from a hydrogen atom and an organic group having 1 to 10 carbon atoms. Two or more of R ^{41 to} R ⁴⁴ may be bonded to each other to form a non-aromatic ring.

ここで、上記式（７）中のＲ⁴³およびＲ⁴⁴は、それぞれ独立に、エーテル結合を含むまたは含まない炭素数１〜１０の置換（例えばハロゲン置換）または無置換のアルキル基であり得る。ｐは、化学結合または炭素数１のアルキレン基であり得る。 Y ⁺ may be an organic cation represented by the following formula (7).

Here, R ⁴³ and R ⁴⁴ in the above formula (7) may each independently be a substituted (for example, halogen-substituted) or unsubstituted alkyl group having 1 to 10 carbon atoms, including or not including an ether bond. p may be a chemical bond or a C 1 alkylene group.

In one preferred embodiment, one or both of R ⁴³ and R ^{44 in} the formula (7) are represented by the following formula (8):
^{-R 1 -O (-R 2 -O)} m -R 3 (8);
It is group represented by these. Here, R ¹ and R ² may each independently be a substituted or unsubstituted alkylene group having 1 to 3 carbon atoms. R ³ may be a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms. m can be 0-2. When a plurality of R ² are contained in the above formula (8), these R ² may be the same or different.

ここで、上記式（９）中のＲ⁵¹〜Ｒ⁵³は、それぞれ独立に、水素原子および炭素数１〜１０の有機基から選択され得る。Ｒ⁵¹とＲ⁵²とは相互に結合して非芳香族性の環を形成していてもよい。 Y ⁺ may be an organic cation represented by the following formula (9).

Here, R ^{51 to} R ⁵³ in the above formula (9) can be independently selected from a hydrogen atom and an organic group having 1 to 10 carbon atoms. R ⁵¹ and R ⁵² may be bonded to each other to form a non-aromatic ring.

Such organic cations and the anion ^{[- N (CORf 1) (} SO 2 Rf 2)] salts with, for example, at least about 30 liquid salt at ° C. (i.e., melting point approximately 30 ° C. The following salts) possible. Further, it may be a salt having a melting point of about 20 ° C. or less. Further, it may be a salt having a melting point of about 0 ° C. or lower (more preferably −20 ° C. or lower). A preferred example of the amide salt disclosed herein is an amide salt in which Y ⁺ in the above formula (1) is an organic cation and is liquid in a temperature range near room temperature (room temperature range). Here, the “room temperature range” is, for example, an upper limit of about 80 ° C. (typically about 60 ° C., and in some cases about 40 ° C.), and a lower limit of about −20 ° C. (typically about 0 ° C., In some cases, it refers to a temperature range of approximately 20 ° C. The amide salt disclosed herein may be an amide salt in which at least a part thereof is in a liquid state (molten state) in at least a part of the temperature range. For example, in a temperature range of at least about 20 to 40 ° C. (more preferably about 0 to 60 ° C., more preferably about −20 to + 80 ° C.), at least a part (preferably all) is in a liquid state (molten state). An amide salt capable of maintaining the above is preferred.

ここで、上記式（１０）中のＲｆ¹は、その化学構造の少なくとも一部にエーテル結合を含むアルキル鎖を有する一価の有機基（典型的には炭化水素基）の全ての水素原子をフッ素原子に置き換えた基（パーフルオロ基）であり得る。Ｒｆ²は、エーテル結合を含むまたは含まない一価の有機基の全ての水素原子をフッ素原子に置き換えた基（パーフルオロ基）であり得る。Ｙ⁺は水素イオン以外のカチオンであり得る。
そのアミド塩製造方法では、次式（１１）：（Ｒｆ¹ＣＯ）₂Ｏ；で表される酸無水物と、次式（１２）：Ｙ^{+ -}ＮＨ（ＳＯ₂Ｒｆ²）；で表されるスルホンアミド塩とを反応させる。ここで、上記式（１１）および（１２）中におけるＲｆ¹，Ｙ⁺およびＲｆ²は、それぞれ上記式（１０）中のＲｆ¹，Ｙ⁺およびＲｆ²と同じである。 According to the present invention, a method for producing an amide salt represented by the following formula (10) is provided.

Here, Rf ¹ in the above formula (10) represents all the hydrogen atoms of a monovalent organic group (typically a hydrocarbon group) having an alkyl chain containing an ether bond in at least a part of its chemical structure. It may be a group (perfluoro group) substituted with a fluorine atom. Rf ² may be a group (perfluoro group) in which all hydrogen atoms of a monovalent organic group containing or not containing an ether bond are replaced with fluorine atoms. Y ⁺ can be a cation other than hydrogen ions.
In its amide salt manufacturing method, the following equation ^{(11) :( Rf 1 CO)} 2 O; and the acid anhydride represented by the following formula ^{(12): Y + - NH} (SO 2 Rf 2); represented by Reaction with a sulfonamide salt. Here, Rf ^1, Y ⁺ and Rf ² in the formula (11) and (12) in each is the same as Rf ^1, Y ⁺ and Rf ² in the above formula (10).

ここで、上記式（１３）中のＲｆ¹は、その化学構造の少なくとも一部にエーテル結合を含むアルキル鎖を有する一価の有機基（典型的には炭化水素基）の全ての水素原子をフッ素原子に置き換えた基（パーフルオロ基）であり得る。Ｒｆ²は、エーテル結合を含むまたは含まない一価の有機基の全ての水素原子をフッ素原子に置き換えた基（パーフルオロ基）であり得る。Ｙ_Ｍ ⁺は金属のカチオンである。
そのアミド塩製造方法では、下記式（１４）：
Ｒｆ¹ＣＯＸ （１４）；
で表される酸ハロゲン化物と、下記式（１５）：
Ｙ_Ｍ ^{+ -}Ｎ（Ｓｉ（Ｒ⁴）₃）（ＳＯ₂Ｒｆ²） （１５）；
で表されるシリルスルホンアミド塩とを反応させる。ここで、上記式（１４）および（１５）中のＲｆ¹，Ｙ_Ｍ ⁺およびＲｆ²は、それぞれ上記式（１３）中のＲｆ¹，Ｙ_Ｍ ⁺およびＲｆ²と同じである。Ｘはハロゲン原子であり得る。Ｒ⁴は、それぞれ独立に、炭素数１〜４のアルキル基であり得る。 Moreover, according to this invention, the method of manufacturing the amide salt represented by following formula (13) is provided.

Here, Rf ¹ in the above formula (13) represents all the hydrogen atoms of a monovalent organic group (typically a hydrocarbon group) having an alkyl chain containing an ether bond in at least a part of its chemical structure. It may be a group (perfluoro group) substituted with a fluorine atom. Rf ² may be a group (perfluoro group) in which all hydrogen atoms of a monovalent organic group containing or not containing an ether bond are replaced with fluorine atoms. Y _M ⁺ is a metal cation.
In the amide salt production method, the following formula (14):
Rf ¹ COX (14);
An acid halide represented by the following formula (15):
_{^{Y M + - N (Si (}} R 4) 3) (SO 2 Rf 2) (15);
Is reacted with a silylsulfonamide salt represented by the formula: Here, Rf ^1, _{Y M} ⁺ and Rf ² in the formula (14) and (15) in are each the same as Rf ^1, _{Y M} ⁺ and Rf ² in the above formula (13). X may be a halogen atom. Each R ⁴ may independently be an alkyl group having 1 to 4 carbon atoms.

ここで、上記式（１６）中のＲｆ¹は、その化学構造の少なくとも一部にエーテル結合を含むアルキル鎖を有する一価の有機基（典型的には炭化水素基）の全ての水素原子をフッ素原子に置き換えた基（パーフルオロ基）であり得る。Ｒｆ²は、エーテル結合を含むまたは含まない一価の有機基の全ての水素原子をフッ素原子に置き換えた基（パーフルオロ基）であり得る。Ｙ⁺は水素イオン以外のカチオンである。
そのアミド塩製造方法では、下記式（１７）：

（Ｒｆ¹およびＲｆ²は、それぞれ、式（１６）中のＲｆ¹およびＲｆ²と同じである。）；
で表されるアミドと、下記式（１８）：
Ｙ^{+ -}ＯＣＯＡ （１８）；
で表される化合物とを反応させる。ここで、上記式（１８）中のＡは、置換または無置換のアルキル基、ヒドロキシ基、および−Ｏ^-Ｙ⁺基からなる群から選択される基であり得る。Ｙ⁺は、上記式（１６）中のＹ⁺と同じである。
ここに開示される製造方法の好ましい態様では、Ｙ⁺がアルカリ金属のカチオン（リチウムイオン、ナトリウムイオン、カリウムイオン等）である。他の好ましい態様では、上記式（１８）で表される塩が炭酸塩および／または炭酸水素塩である。 Moreover, according to this invention, the method of manufacturing the amide salt represented by following formula (16) is provided.

Here, Rf ¹ in the above formula (16) represents all the hydrogen atoms of a monovalent organic group (typically a hydrocarbon group) having an alkyl chain containing an ether bond in at least a part of its chemical structure. It may be a group (perfluoro group) substituted with a fluorine atom. Rf ² may be a group (perfluoro group) in which all hydrogen atoms of a monovalent organic group containing or not containing an ether bond are replaced with fluorine atoms. Y ⁺ is a cation other than hydrogen ions.
In the amide salt production method, the following formula (17):

(Rf ¹ and Rf ² are the same as Rf ¹ and Rf ^{2 in} formula (16), respectively);
An amide represented by the following formula (18):
Y ^{+ -} OCOA (18);
The compound represented by these is made to react. Here, A in the formula (18) may be a group selected from the group consisting of a substituted or unsubstituted alkyl group, a hydroxy group, and an —O ⁻ Y ⁺ group. Y ⁺ is the same as Y ⁺ in the formula (16).
In a preferred embodiment of the production method disclosed herein, Y ⁺ is an alkali metal cation (lithium ion, sodium ion, potassium ion, etc.). In another preferred embodiment, the salt represented by the formula (18) is a carbonate and / or bicarbonate.

ここで、上記式（１９）中のＲｆ¹は、その化学構造の少なくとも一部にエーテル結合を含むアルキル鎖を有する一価の有機基（典型的には炭化水素基）の全ての水素原子をフッ素原子に置き換えた基（パーフルオロ基）であり得る。Ｒｆ²は、エーテル結合を含むまたは含まない一価の有機基の全ての水素原子をフッ素原子に置き換えた基（パーフルオロ基）であり得る。Ｙ_Ｏ ⁺は有機カチオンである。
そのアミド塩製造方法では、下記式（２０）：

（Ｒｆ¹およびＲｆ²は、それぞれ、式（１９）中のＲｆ¹およびＲｆ²と同じである。Ｙ_Ｍ ⁺は金属のカチオンである。）；
で表されるアミド塩と、下記式（２１）：
Ｙ_Ｏ ^{+ -}Ｂ （２１）；
で表される化合物とを反応させる。ここで、上記式（２１）中のＹ_Ｏ ⁺は、上記式（１９）中のＹ_Ｏ ⁺と同じである。^-Ｂは無機または有機のアニオンであり得る。 Moreover, according to this invention, the method of manufacturing the amide salt represented by following formula (19) is provided.

Here, Rf ¹ in the above formula (19) represents all the hydrogen atoms of a monovalent organic group (typically a hydrocarbon group) having an alkyl chain containing an ether bond in at least a part of its chemical structure. It may be a group (perfluoro group) substituted with a fluorine atom. Rf ² may be a group (perfluoro group) in which all hydrogen atoms of a monovalent organic group containing or not containing an ether bond are replaced with fluorine atoms. Y 2 _O ⁺ is an organic cation.
In the amide salt production method, the following formula (20):

(Rf ¹ and Rf ² are the same as Rf ¹ and Rf ^{2 in} formula (19), respectively. Y _M ⁺ is a metal cation.);
An amide salt represented by the following formula (21):
_{^{Y O + - B (21)}} ;
The compound represented by these is made to react. Here, _{Y O} ⁺ is in the formula (21) is the same as _{Y O} ⁺ in the formula (19). ^- B can be an anion of an inorganic or organic.

ここで、上記式（２２）におけるＲｆ¹は、その化学構造の少なくとも一部にエーテル結合を含むアルキル鎖を有する有機基（典型的には炭化水素基）の全ての水素原子をフッ素原子に置き換えた基であり得る。例えば、エーテル結合を含む炭素数２〜１０（好ましくは２〜５）のパーフルオロアルキル基であり得る。ここに開示されるアミドの好ましい一つの態様では、Ｒｆ¹が、下記式（２３）：
−Ｒｆ³−Ｏ（−Ｒｆ⁴−Ｏ）_n−Ｒｆ⁵ （２３）；
で表される基である。式（２３）中のＲｆ³およびＲｆ⁴は、それぞれ独立に、炭素数１〜３のパーフルオロアルキレン基であり得る。Ｒｆ⁵は、炭素数１〜５のパーフルオロアルキル基であり得る。ｎは０〜２の数であり得る。上記式（２３）中に複数のＲｆ⁴が含まれる場合、それらのＲｆ⁴は同一であってもよく異なっていてもよい。
また、上記式（２２）におけるＲｆ²は、エーテル結合を含むまたは含まない有機基の全ての水素原子をフッ素原子に置き換えた基であり得る。Ｒｆ²の好適例としては、炭素数１〜５のパーフルオロアルキル基（例えばトリフルオロメチル基）が挙げられる。
このようなアミドは、例えば、上記式（１８）で表される化合物と反応させて上記式（１６）で表されるアミド塩を製造する上記方法に使用するアミドとして好適である。換言すれば、アミド塩製造用の原料（中間体）として有用である。 Furthermore, according to the present invention, an amide represented by the following formula (22) is provided.

Here, Rf ¹ in the above formula (22) replaces all hydrogen atoms of an organic group (typically a hydrocarbon group) having an alkyl chain containing an ether bond in at least a part of its chemical structure with a fluorine atom. Group. For example, it may be a C 2-10 (preferably 2-5) perfluoroalkyl group containing an ether bond. In one preferred embodiment of the amide disclosed herein, Rf ¹ is represented by the following formula (23):
^{-Rf 3 -O (-Rf 4 -O)} n -Rf 5 (23);
It is group represented by these. Rf ³ and Rf ^{4 in} formula (23) may each independently be a C 1 to C 3 perfluoroalkylene group. Rf ⁵ may be a C 1-5 perfluoroalkyl group. n may be a number from 0-2. When the formula (23) includes a plurality of Rf ⁴ , these Rf ⁴ may be the same or different.
In addition, Rf ² in the above formula (22) may be a group in which all hydrogen atoms of an organic group including or not including an ether bond are replaced with fluorine atoms. Preferred examples of Rf ^2, include perfluoroalkyl group having 1 to 5 carbon atoms (e.g., trifluoromethyl group).
Such an amide is suitable, for example, as an amide used in the above method for producing an amide salt represented by the above formula (16) by reacting with a compound represented by the above formula (18). In other words, it is useful as a raw material (intermediate) for producing an amide salt.

ここで、上記式（２４）中のＲｆ¹は、その化学構造の少なくとも一部にエーテル結合を含むアルキル鎖を有する一価の有機基（典型的には炭化水素基）の全ての水素原子をフッ素原子に置き換えた基であり得る。Ｒｆ²は、エーテル結合を含むまたは含まない一価の有機基の全ての水素原子をフッ素原子に置き換えた基であり得る。
そのアミド製造方法では、下記式（２５）：

（Ｒｆ¹およびＲｆ²は、それぞれ、式（２４）中のＲｆ¹およびＲｆ²と同じである。Ｙ⁺は水素イオン以外のカチオンである。）；
で表されるアミド塩と酸（好ましくは強酸、例えば硫酸）とを反応させる。 According to the present invention, a method for producing an amide represented by the following formula (24) is provided.

Here, Rf ¹ in the above formula (24) represents all the hydrogen atoms of a monovalent organic group (typically a hydrocarbon group) having an alkyl chain containing an ether bond in at least a part of its chemical structure. It may be a group substituted with a fluorine atom. Rf ² may be a group in which all hydrogen atoms of a monovalent organic group containing or not containing an ether bond are replaced with fluorine atoms.
In the amide production method, the following formula (25):

(Rf ¹ and Rf ² are the same as Rf ¹ and Rf ^{2 in} formula (24), respectively. Y ⁺ is a cation other than a hydrogen ion);
And an acid (preferably a strong acid such as sulfuric acid).

The amide produced by such a method is suitable, for example, as an amide used in the above-mentioned method for producing an amide salt represented by the above formula (16) by reacting with a compound represented by the above formula (18).
In addition, the amide salt represented by the above formula (1) can be suitably produced by carrying out any one of the amide salt production methods described above alone or in appropriate combination. Alternatively, it can be preferably produced by carrying out any combination of the above-mentioned amide salt production method and amide production method as appropriate.

According to the present invention, an electrolyte containing one or more of the amide salts described above is provided. As a preferred example of such an electrolyte, an electrolyte containing one or more amide salts in which Y ⁺ in the above formula (1) is an organic cation can be mentioned. In one preferred embodiment of the electrolyte disclosed herein, Y ⁺ is an organic cation, and the electrolyte is mainly composed of a liquid (molten) amide salt in at least a part of the normal temperature range. For example, it is preferable that the main component is a liquid amide salt at least at about 30 ° C. (more preferably about 20 ° C., further preferably about 0 ° C., particularly preferably −20 ° C.).
The electrolyte disclosed herein can contain an inorganic or organic lithium salt in addition to such a liquid amide salt. The lithium salt may be an amide lithium salt in which Y ⁺ in the above formula (1) is a lithium ion (Li ⁺ ). An electrolyte containing such a lithium salt, which is a liquid electrolyte at normal temperature, is preferable. For example, a liquid electrolyte is preferred at least about 30 ° C. (more preferably about 20 ° C., further preferably about 0 ° C., particularly preferably −20 ° C.). One preferred embodiment of such an electrolyte is a liquid in which the above amide lithium salt (supporting salt) is dissolved in a liquid amide salt (medium) in at least a part of the normal temperature range where Y ⁺ is an organic cation. It is an electrolyte.

  In addition, according to the present invention, an electricity storage device including any one of the above-described electrolytes is provided. Here, the “storage element” refers to various electrochemical batteries (including primary batteries and secondary batteries. Examples include lithium ion batteries and nickel metal hydride batteries) and capacitors (for example, electric double layer capacitors). It is a concept that includes both of them. According to the present invention, a lithium ion secondary battery comprising any one of the above-described electrolytes is provided. In one preferred embodiment of such a battery, the battery includes an electrolyte that is liquid at room temperature. For example, it is preferable to provide an electrolyte that is liquid at least at about 30 ° C. (preferably about 20 ° C., more preferably about 0 ° C., particularly preferably about −20 ° C.).

An aspect of the invention disclosed herein is an ion conductive material containing one or more of the amide salts described above. It is preferable that it is a liquid ion conductive material in the said normal temperature range. Such an ion conductive material can be used, for example, as a component of an electric storage element or other various electrochemical devices. Moreover, it can utilize as electrolytes, such as photochemical cells, such as a solar cell, and power generators, such as a fuel cell, or its component.
Still another aspect of the invention disclosed herein is a medium containing one or more of the amide salts described above. The medium is preferably a liquid medium in the normal temperature range. Such a medium can be preferably used for various applications as, for example, a nonflammable solvent, a non-volatile solvent, and the like. For example, it can be useful as a solvent (electrolyte medium) for dissolving a supporting salt (lithium salt or the like) in an electrolyte of a non-aqueous battery (lithium ion secondary battery or the like).

  Hereinafter, preferred embodiments of the present invention will be described in detail. It should be noted that technical matters other than the contents particularly mentioned in the present specification and necessary for the implementation of the present invention can be grasped as design matters of those skilled in the art based on the prior art. The present invention can be carried out based on the technical contents disclosed in the present specification and the common general technical knowledge in the field.

<About the anion component>
Amide salt represented by the above formula (1) ^is - including N (CorF ¹⁾ anion component represented by (SO ₂ Rf ^2). This anion component has a structure in which a sulfonyl group (—SO ₂ —) and a carbonyl group (—CO—) are bonded to one nitrogen atom (N). A perfluoro group (typically a perfluorohydrocarbon group) Rf ¹ containing an ether bond is bonded to the carbonyl group. A perfluoro group (typically a perfluorohydrocarbon group) Rf ² with or without an ether bond is bonded to the sulfonyl group. Thus, in the anion component, both the sulfonyl group and carbonyl group bonded to the nitrogen atom have a perfluoro group.

The perfluoro group (Rf ¹ ) bonded to the carbonyl group (—CO—) is a perfluoroalkyl chain (perfluoroalkyl ether chain) containing one or more ether bonds in at least a part of its chemical structure. ). That is, Rf ¹ has a structure containing a perfluoroalkyl chain into which one or two or more ether bonds (C—O—C bonds) are introduced (therefore, the perfluoroalkyl chain has 2 or more carbon atoms, Rf ¹ is a perfluoroalkyl group having 2 or more carbon atoms. This perfluoroalkyl ether chain may be an open chain or may form a ring structure. As used herein, “open chain” is a concept including both an open chain having no branch (straight chain) and an open chain having a branch (branched chain) unless otherwise specified. Rf ¹ having an open chain (that is, linear or branched) perfluoroalkyl ether chain is preferred. The perfluoroalkyl ether chain can have other substituents. For example, perfluorohydrocarbon groups other than perfluoroalkyl groups (for example, perfluorohydrocarbon groups such as perfluorovinyl groups, perfluorohydrocarbon groups, perfluorophenyl groups, perfluorobenzyl groups, perfluorobenzyl groups, and other perfluorohydrocarbon groups). A perfluoroalkyl ether chain having a substituent such as a perfluoro group containing an element other than fluorine and carbon (for example, O, N, S, P, etc.). A particularly preferred perfluoroalkyl ether chain contained in Rf ¹ is an open chain perfluoroalkyl ether chain having no other substituent.

The anion constituting the amide salt represented by the above formula (1) may be an anion having a structure in which such a perfluoroalkyl ether chain is directly bonded to a carbonyl group. Further, such a perfluoroalkyl ether chain may be bonded to the carbonyl group via another perfluoro group. For example, the perfluoroalkyl ether chain may be a perfluorohydrocarbon group (for example, an unsaturated perfluorohydrocarbon group such as a perfluorovinylene group or an aromatic perfluorohydrocarbon group such as a perfluorophenylene group). Etc.) and an anion having a structure bonded to the carbonyl group. The perfluoroalkyl ether chain may be an anion having a structure in which the perfluoroalkyl ether chain is bonded to a carbonyl group via a perfluoro group containing an element other than fluorine and carbon (for example, O, N, S, P, etc.). A preferred example of the anion constituting the amide salt disclosed herein is an anion having a structure in which a perfluoroalkyl ether chain is directly bonded to a carbonyl group (that is, Rf ¹ is a perfluoroalkyl ether group). A perfluoroalkyl ether group having no other substituent is preferred. Further, a linear or branched perfluoroalkyl ether group is preferable.

The total number (carbon number) of carbon atoms contained in Rf ¹ may be 2 to 16, for example. The carbon number is preferably 2 to 10, and more preferably 2 to 5. The number of ether bonds contained in Rf ¹ can be, for example, 1-5. The number of ether bonds is preferably 1 to 3. Preferable examples of Rf ¹ include perfluoroalkyl ether groups that satisfy the above carbon number and the number of ether bonds, are linear or branched, and have no other substituent.

Rf ¹ is represented by the following formula (2):
^{-Rf 3 -O (-Rf 4 -O)} n -Rf 5 (2);
The perfluoroalkyl ether group represented by these may be sufficient. Here, Rf ³ and Rf ⁴ may each independently be a linear or branched perfluoroalkylene group having 1 to 3 carbon atoms. Rf ⁵ may be a linear or branched perfluoroalkyl group having 1 to 5 carbon atoms. n may be a number from 0 to 4 (preferably 0 to 2). When a plurality of Rf ⁴ are contained in the above formula (2), these Rf ⁴ may be the same or different. Rf ³ , Rf ⁴ and Rf ⁵ preferably do not have any other substituents.

In a preferred embodiment of the amide salt disclosed herein, the Rf ¹ is —CF ₂ OCF ₃ , —CF ₂ OCF ₂ CF ₃ , —CF ₂ OCF ₂ CF ₂ CF ₃ , —CF ₂ CF ₂ OCF ₃ , _{-CF 2 CF 2 OCF 2 CF 3} , -CF 2 CF 2 CF 2 OCF 3, -CF 2 OCF 2 CF 2 OCF 3, -CF 2 CF 2 OCF 2 CF 2 OCF 3, -CF (CF 3) OCF 3 , —CF (CF ₃ ) OCF ₂ CF ₃ , —CF (CF ₃ ) OCF ₂ CF ₂ CF ₃ , and —C (CF ₃ ) ₂ OCF ₃ . Among these, more preferable Rf ¹ is -CF ₂ OCF ₃ , -CF ₂ OCF ₂ CF ₃ , -CF ₂ CF ₂ OCF ₃ , -CF ₂ CF ₂ OCF ₂ CF ₃ , -CF ₂ CF ₂ CF ₂ OCF ₃ , —CF ₂ OCF ₂ CF ₂ OCF ₃ , —CF ₂ CF ₂ OCF ₂ CF ₂ OCF ₃ , —CF (CF ₃ ) OCF ₃ , —CF (CF ₃ ) OCF ₂ CF ₃ , and —CF (CF ₃₎ OCF ₂ CF ₂ CF ₃ and the like. As particularly preferred Rf ¹ , —CF ₂ OCF ₃ , —CF ₂ OCF ₂ CF ₃ , —CF ₂ CF ₂ OCF ₃ , —CF ₂ OCF ₂ CF ₂ OCF ₃ , and —CF (CF ₃ ) OCF ₂ CF ₂ CF ₃ is mentioned.

On the other hand, the perfluoro group (Rf ² ) bonded to the sulfonyl group (—SO ₂ —) may be a perfluoro hydrocarbon group including or not including an ether bond. For example, it may be a perfluoroalkyl group with or without an ether bond. The perfluoroalkyl group or perfluoroalkyl ether group may be an open chain or may form a ring structure. An open chain (linear or branched) perfluoroalkyl group is preferred. The perfluoroalkyl or perfluoroalkyl ether group may or may not have other substituents. In the case of having another substituent, the substituent is a perfluoro hydrocarbon group other than a perfluoroalkyl group, a perfluoro group containing an element other than fluorine and carbon (for example, O, N, S, P, etc.), etc. It may be a perfluoroalkyl group having a group. A perfluoroalkyl group having no other substituent is preferred. For example, it is preferably a linear or branched perfluoroalkyl group that does not contain an ether bond and has no other substituent.

The total number (carbon number) of carbon atoms contained in Rf ² may be 1 to 10, for example. The carbon number is preferably 1 to 5, and more preferably 1 to 3. Preferable examples of Rf ² include perfluoroalkyl groups that satisfy the above carbon number, are linear or branched (more preferably linear), and have no other substituent. Specific examples of such perfluoroalkyl groups include —CF ₃ , —CF ₂ CF ₃ , —CF ₂ CF ₂ CF ₃ , —CF ₂ (CF ₂ ) ₂ CF ₃ , and —CF ₂ (CF _{2 4} CF ₃ is mentioned. Of these, —CF ₃ , —CF ₂ CF ₃ , and —CF ₂ CF ₂ CF ₃ are preferable. It is particularly preferred that Rf ² is —CF ₃ .

<Cation component>
The amide salt represented by the formula (1) includes a cation component represented by Y ⁺ . The cation component may be an inorganic cation or an organic cation. For example, it may be a monovalent organic cation containing at least one element selected from nitrogen (N), sulfur (S), oxygen (O) and phosphorus (P). For example, it may be an organic cation having a structure in which one or two or more organic groups are bonded to at least one of the elements (any of N, S, O and P) contained in the cation. One preferred example of such an organic group is an open chain (for example, straight chain) alkyl group having 1 to 10 carbon atoms (preferably 1 to 6 carbon atoms) and including or not including an ether bond. Can be mentioned. The cation component may be an organic cation composed of at least one element other than N, S, O, and P and having a lone electron pair in a neutral state.

[Imidazolium ions]
A preferred example of Y ⁺ is an imidazolium ion represented by the above formula (3). R ^{11 to} R ¹⁵ may be independently selected from a hydrogen atom, a halogen atom, and an organic group having 1 to 10 carbon atoms. Two or more of R ^{11 to} R ¹⁵ may be bonded to each other to form a ring structure. In this case, these groups may form a ring structure with an oxygen atom interposed therebetween, or may form a ring structure without an oxygen atom interposed (that is, without intervening). Typically, at least one of the nitrogen atoms constituting the imidazole ring has an organic group having 1 to 10 carbon atoms. In other words, at least one (preferably both) of R ¹¹ and R ¹³ is an organic group having 1 to 10 carbon atoms.

When any of R ^{11 to} R ¹⁵ is a halogen atom, the halogen atom can be selected from the group consisting of F, Cl, Br and I. Further, when any of R ^{11 to} R ¹⁵ is the organic group, the organic group may be a hydrocarbon group that includes or does not include an ether bond. The hydrocarbon group may be in an open chain or may form a ring structure. The hydrocarbon group may be either saturated or unsaturated. When the hydrocarbon group forms a ring structure, the ring may be aromatic or non-aromatic. In the hydrocarbon group, part or all of the hydrogen atoms may be substituted with a halogen atom (for example, one or more halogen atoms selected from the group consisting of F, Cl, Br and I). . Examples of such halogen-substituted hydrocarbon groups include fluoroalkyl groups that are partially substituted with fluorine atoms, with or without ether linkages. Other examples include perfluoroalkyl groups that are perfluorinated and contain or do not contain ether linkages (ie, perfluoroalkyl groups that contain or do not contain ether linkages).

In a preferred example of the cation represented by the above formula (3), R ^{11 to} R ¹⁵ may be independently selected from a hydrogen atom and a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms. The alkyl group may be an open chain or may form a ring structure. An open-chain alkyl group is preferable, and a linear alkyl group is more preferable. When the alkyl group is an alkyl group having a substituent (that is, a substituted alkyl group), the substituent can be a halogen atom. For example, it may be one or more halogen atoms (preferably fluorine atoms) selected from the group consisting of F, Cl, Br and I. In one preferred embodiment, R ^{11 to} R ¹⁵ are each independently selected from a hydrogen atom and a substituted or unsubstituted (preferably unsubstituted) open-chain alkyl group having 1 to 4 carbon atoms. Examples of such alkyl groups include —CH ₃ , —CH ₂ CH ₃ , —CH ₂ CH ₂ CH ₃ , —CH ₂ CH ₂ CH ₂ CH ₃ , —CH (CH ₃ ) CH ₃ , —CH (CH _{3 ) CH 2 CH 3, -CH 2} CH (CH 3) CH 3, and the like _{-C (CH 3) 2 CH 3} . Of these, —CH ₃ , —CH ₂ CH ₃ , and —CH ₂ CH ₂ CH ₃ are particularly preferred.

In a preferred example of the cation represented by the above formula (3), a group (that is, R ¹¹ and R ¹³ ) bonded to nitrogen constituting the imidazole ring among R ^{11 to} R ¹⁵ is independently It may be selected from alkyl groups having 1 to 4 carbon atoms. Moreover, the group (namely, R < ¹² >, R <^14> and R <^15> ) couple | bonded with carbon which comprises an imidazole ring may be selected from a hydrogen atom and a C1-C4 alkyl group each independently. For example, all the groups (R ¹¹ , R ¹² , R ¹³ ) bonded to the 1-position, 2-position and 3-position of the imidazole ring may be imidazolium ions, which are alkyl groups having 1 to 4 carbon atoms. In addition, the groups (R ¹¹ , R ¹² , R ¹³ ) bonded to the 1-position, 2-position and 3-position of the imidazole ring are alkyl groups having 1 to 4 carbon atoms, and are bonded to the 4-position and 5-position. One or both of the selected groups (R ¹⁴ , R ¹⁵ ) may be an imidazolium ion which is an alkyl group having 1 to 4 carbon atoms.

  Specific examples of the cation represented by the above formula (3) include 1,3-dimethylimidazolium ion, 1,3-diethylimidazolium ion, 1,3-dipropylimidazolium ion, 1-ethyl-3- Dialkylimidazolium ions such as methylimidazolium ion, 1-methyl-3-propylimidazolium ion, 1-isopropyl-3-propylimidazolium ion; 1,2,3-trimethylimidazolium ion, 1,2,3 Trialkylimidazolium ions such as triethylimidazolium ion, 1-ethyl-2,3-dimethylimidazolium ion, 1,2-dimethyl-3-propylimidazolium ion, 2-ethyl-1,3-dimethylimidazolium ion Ions: 1,2,3,4-tetramethylimidazolium ion 1,2,3,4-tetraethylimidazolium ion, tetraalkylimidazolium ions such as 2-ethyl-1,3,4-trimethylimidazolium ion; 1,2,3,4,5-pentamethylimidazole And pentaalkylimidazolium ions such as 1-ethyl-2,3,4,5-tetramethylimidazolium ion; and the like.

[Pyridinium ions]
Another preferred example of Y ⁺ is a pyridinium ion represented by the above formula (4). R ^{21 to} R ²⁶ may be independently selected from a hydrogen atom, a halogen atom (for example, F, Cl, Br, I) and an organic group having 1 to 10 carbon atoms. Two or more of R ^{21 to} R ²⁶ may be bonded to each other to form a ring structure. In this case, these groups may form a ring structure with an oxygen atom interposed, or may form a ring structure without an oxygen atom. Typically, the nitrogen atom constituting the pyridine ring has an organic group having 1 to 10 carbon atoms. That is, R ²¹ is an organic group having 1 to 10 carbon atoms.
When any of R ^{21 to} R ²⁶ is the organic group, the organic group may be the same group as R ^{11 to} R ¹⁵ described above. For example, it may be a hydrocarbon group with or without an ether bond. Further, it may be a substituted or unsubstituted hydrocarbon group. Further, it may be a hydrocarbon group having an open chain or ring structure. When any of R ^{21 to} R ²⁶ is a hydrocarbon group, preferred examples thereof are substituted or unsubstituted having 1 to 10 carbon atoms (more preferably 1 to 4 carbon atoms) and including or not containing an ether bond. An alkyl group is mentioned. An open chain alkyl group is preferred. Moreover, an unsubstituted alkyl group is preferable. Examples of particularly preferred alkyl groups include —CH ₃ , —CH ₂ CH ₃ , and —CH ₂ CH ₂ CH ₃ .
In a preferred embodiment, the group (R ²¹ ) bonded to the nitrogen constituting the pyridine ring is an alkyl group having 1 to 10 carbon atoms (more preferably 1 to 4 carbon atoms). R ^{22 to} R ²⁶ are each independently selected from a hydrogen atom and an alkyl group having 1 to 10 (more preferably 1 to 4) carbon atoms. Typically, R ^{22 to} R ²⁶ are all hydrogen atoms. Specific examples of the cation represented by the above formula (4) include N-methylpyridinium ion, N-ethylpyridinium ion, N-propylpyridinium ion, N-isopropylpyridinium ion, and N-butylpyridinium ion. .

[Oxazolium ions]
Another suitable example of Y ⁺ is an oxazolium ion represented by the above formula (5). R ^{31 to} R ³⁴ may be independently selected from a hydrogen atom, a halogen atom (for example, F, Cl, Br, I) and an organic group having 1 to 10 carbon atoms. Two or more of R ^{31 to} R ³⁴ may be bonded to each other via an oxygen atom or non-intervening oxygen atom to form a ring structure. Typically, the nitrogen atom constituting the oxazole ring has an organic group having 1 to 10 carbon atoms. That is, R ³² is an organic group having 1 to 10 carbon atoms.
When any of R ^{31 to} R ³⁴ is the organic group, the organic group can be the same group as R ^{11 to} R ¹⁵ described above. For example, it may be a hydrocarbon group with or without an ether bond. Further, it may be a substituted or unsubstituted hydrocarbon group. Further, it may be a hydrocarbon group having an open chain or ring structure. When any of R ^{31 to} R ³⁴ is a hydrocarbon group, preferred examples thereof are substituted or unsubstituted, having or not containing an ether bond, having 1 to 10 carbon atoms (more preferably 1 to 4 carbon atoms). An alkyl group is mentioned. An open chain alkyl group is preferred. Moreover, an unsubstituted alkyl group is preferable. Examples of particularly preferred alkyl groups include —CH ₃ , —CH ₂ CH ₃ , and —CH ₂ CH ₂ CH ₃ .
In one preferred embodiment, the group (R ³² ) bonded to the nitrogen constituting the oxazole ring is an alkyl group having 1 to 10 (more preferably 1 to 4) carbon atoms. R ³¹ , R ³³ , and R ³⁴ are each independently selected from a hydrogen atom and an alkyl group having 1 to 10 (more preferably 1 to 4) carbon atoms. Typically, R ³¹ , R ³³ , and R ³⁴ are all hydrogen atoms. Specific examples of the cation represented by the above formula (5) include N-methyloxazolium ion, N-ethyloxazolium ion, and N-propyloxazolium ion.

[Ammonium ions]
Another preferred example of Y ⁺ is an ammonium ion represented by the above formula (6). At least one of R ^{41 to} R ⁴⁴ may be selected from an organic group having 1 to 10 carbon atoms, and the other may be independently selected from a hydrogen atom and an organic group having 1 to 10 carbon atoms. It is preferable that two or more (more preferably three or more) of R ^{41 to} R ⁴⁴ are organic groups having 1 to 10 carbon atoms. Typically, R ^{41 to} R ⁴⁴ are all organic groups having 1 to 10 carbon atoms. Two or more of R ^{41 to} R ⁴⁴ may be bonded to each other through an oxygen atom or non-oxygen atom to form a non-aromatic ring.
When any of R ^{41 to} R ⁴⁴ is the organic group, the organic group can be the same group as R ^{11 to} R ¹⁵ described above. For example, it may be a hydrocarbon group with or without an ether bond. Further, it may be a substituted or unsubstituted hydrocarbon group. Further, it may be a hydrocarbon group having an open chain or ring structure. When any of R ^{41 to} R ⁴⁴ is a hydrocarbon group, preferred examples thereof include substituted or unsubstituted (preferably unsubstituted) alkyl having 1 to 10 carbon atoms and containing or not containing an ether bond. Group or alkenyl group. As a preferred example of R ^{41 to} R ⁴⁴ , an open chain (preferably linear) having 1 to 4 carbon atoms such as —CH ₃ , —CH ₂ CH ₃ , and —CH ₂ CH ₂ CH _3. An alkyl group is mentioned. Other preferable examples of R ^{41 to} R ⁴⁴ include an open-chain (preferably linear) alkyl group having 2 to 10 carbon atoms (more preferably 2 to 5 carbon atoms) containing one or more ether bonds. It is done.

Specific examples of the cation represented by the above formula (6) include R ^{41 to} R ⁴⁴ having the same alkyl group such as tetramethylammonium ion, tetraethylammonium ion, tetrapropylammonium ion and tetrabutylammonium ion. Some tetraalkylammonium ions are mentioned. Other examples include ethyl trimethylammonium ion, triethylmethylammonium ion, diethyldimethylammonium ion, trimethylpropylammonium ion, triethylpropylammonium ion, trimethylisopropylammonium ion, triethylisopropylammonium ion, dimethyldipropylammonium ion, butyltrimethylammonium ion And tetraalkylammonium ions in which R ^{41 to} R ⁴⁴ are two or more alkyl groups, such as tributylmethylammonium ion. Still other examples include ammonium ions in which R ^{41 to} R ⁴⁴ are an alkyl group and an alkylene group, such as vinyl trimethyl ammonium ion and allyl trimethyl ammonium ion. As still another example, at least one of R ^{41 to} R ⁴⁴ such as 2-methoxyethyltrimethylammonium ion, 2-ethoxyethyltrimethylammonium ion, 2-methoxyethyltriethylammonium ion, etc. Ammonium ions which are ether groups) and others are alkyl groups.

Two or more of R ^{41 to} R ⁴⁴ may be bonded to each other to form a non-aromatic ring. Such non-aromatic rings can be aliphatic rings containing a nitrogen atom. For example, it may be an aliphatic five-membered ring containing a nitrogen atom (pyrrolidine ring), an aliphatic six-membered ring containing a nitrogen atom (piperidine ring), or the like. The carbon atoms constituting the ring may or may not have a substituent. In the case of having a substituent, the substituent is a halogen atom (for example, F, Cl, Br, I, preferably F.), an alkyl group having 1 to 4 carbon atoms, and a part or all of hydrogen atoms of the alkyl group. Or a group in which is substituted with a halogen atom. The cation represented by the above formula (6) has a structure in which two of R ^{41 to} R ⁴⁴ (for example, R ⁴¹ and R ⁴² ) are bonded to each other to form a pyrrolidine ring or piperidine ring having no substituent. Of ammonium ions (ie, pyrrolidinium ions or piperidinium ions). The remaining group may be a substituted or unsubstituted (preferably unsubstituted) alkyl or alkenyl group having 1 to 10 carbon atoms (more preferably 1 to 4 carbon atoms) and including or not including an ether bond.

A preferred example of Y ⁺ is a cation represented by the above formula (7). The cation becomes a pyrrolidinium ion when p is a chemical bond, and becomes a piperidinium ion when p is an alkylene group having 1 carbon atom (that is, a methylene group). R ⁴³ and R ⁴⁴ may each independently be a substituted or unsubstituted alkyl group having 1 to 10 carbon atoms that includes or does not include an ether bond. Preferable examples of the group that can be selected as R ⁴³ and R ⁴⁴ include an open chain (preferably linear) alkyl group having 1 to 4 carbon atoms, and 2 to 10 carbon atoms containing one or more ether bonds. (More preferably 2 to 5) open chain (preferably linear) alkyl group and the like.
In one preferred embodiment, one or both of R ⁴³ and R ⁴⁴ is a group represented by the above formula (8). R ¹ and R ² may each independently be a substituted or unsubstituted alkylene group having 1 to 3 carbon atoms. R ³ may be a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms. Examples of the substituent that R ^{1 to} R ³ may have include a halogen atom (eg, F, Cl, Br, I). R ^{1 to} R ³ are each preferably an alkylene group or an alkyl group having no substituent. Moreover, it is preferable that all of R ^{1 to} R ³ are open chain (preferably linear) alkylene groups or alkyl groups. The group represented by the above formula (8) may contain one (m = 0) to three (m = 2) ether bonds. It is preferable that m is 0-1. When a plurality of R ² are contained in the above formula (8), these R ² may be the same or different.

Specific examples of the cation represented by the formula (7) include N, N-dimethylpyrrolidinium ion, N-ethyl-N-methylpyrrolidinium ion, N-methyl-N-propylpyrrolidinium ion, and N-butyl. Examples thereof include dialkylpyrrolidinium ions and dialkylpiperidinium ions such as -N-methylpyrrolidinium ion, N, N-dimethylpiperidinium ion and N-methyl-N-propylpiperidinium ion. Also, one of R ⁴³ and R ⁴⁴ is CH ₃ OCH ₂ CH ₂ —, CH ₃ CH ₂ OCH ₂ CH ₂ —, CH ₃ OCH ₂ CH ₂ OCH ₂ CH ₂ —, and CH ₃ CH ₂ OCH ₂ CH ₂ OCH. ₂ pyrrolidinyl which is any alkyl ether group selected from —CH ₂ — and the other is any alkyl group selected from —CH ₃ , —CH ₂ CH ₃ , and —CH ₂ CH ₂ CH ₃ Umum ion or piperidinium ion may be used. Both R ⁴³ and R ⁴⁴ are independently CH ₃ OCH ₂ CH ₂ —, CH ₃ CH ₂ OCH ₂ CH ₂ —, CH ₃ OCH ₂ CH ₂ OCH ₂ CH ₂ —, and CH ₃ CH ₂ OCH _2. It may be a pyrrolidinium ion or piperidinium ion which is any alkyl ether group selected from CH ₂ OCH ₂ CH ₂ —.

[Sulphonium ions]
Another preferred example of Y ⁺ is a sulfonium ion represented by the above formula (9). At least one of R ^{51 to} R ⁵³ may be selected from an organic group having 1 to 10 carbon atoms, and the other may be independently selected from a hydrogen atom and an organic group having 1 to 10 carbon atoms. It is preferable that two or more of R ^{51 to} R ⁵³ are organic groups having 1 to 10 carbon atoms. Typically, each of R ^{51 to} R ⁵³ is an organic group having 1 to 10 carbon atoms. Two or more of R ^{51 to} R ⁵³ may be bonded to each other via an oxygen atom or non-oxygen atom to form a non-aromatic ring.
When any of R ^{51 to} R ⁵³ is the organic group, the organic group can be the same group as R ^{11 to} R ¹⁵ described above. For example, it may be a hydrocarbon group with or without an ether bond. Further, it may be a substituted or unsubstituted hydrocarbon group. Further, it may be a hydrocarbon group having an open chain or ring structure. When any of R ^{51 to} R ⁵³ is a hydrocarbon group, preferred examples thereof are substituted or unsubstituted, having 1 to 10 carbon atoms (more preferably 1 to 4), containing or not containing an ether bond. An alkyl group is mentioned. An open chain alkyl group is preferred. Moreover, an unsubstituted alkyl group is preferable. Examples of particularly preferred alkyl groups include —CH ₃ , —CH ₂ CH ₃ , and —CH ₂ CH ₂ CH ₃ . Specific examples of the cation represented by the formula (9) include trialkylsulfonium ions such as trimethylsulfonium ion, triethylsulfonium ion, tripropylsulfonium ion, tributylsulfonium ion, diethylmethylsulfonium ion, dimethylpropylsulfonium ion, And triarylsulfonium ions such as triphenylsulfonium ion.

[Other organic cations]
Y ⁺ can also be a thiazolium ion, an isoxazolium ion, a triazolium ion, a pyridazinium ion, a pyrimidinium ion, or a pyrazinium ion. In these ions, typically, a nitrogen atom constituting a heterocyclic ring (at least one of those nitrogen atoms in a ring containing two or more nitrogen atoms) is an organic group having 1 to 10 carbon atoms as a substituent. Has a group. The organic group has, for example, an open-chain alkyl group having 1 to 10 carbon atoms (preferably 1 to 4) and including or not including an ether bond. On the other hand, other atoms (for example, carbon atoms) constituting the heterocyclic ring may or may not have a substituent. When it has a substituent, the substituent may be selected from a halogen atom (for example, F, Cl, Br, I, preferably F.) and an organic group having 1 to 10 carbon atoms. The organic group may be, for example, an open-chain alkyl group having 1 to 10 carbon atoms (preferably 1 to 4) and including or not including an ether bond.
Y ⁺ may be a phosphonium cation having a structure in which the nitrogen atom (N) in the above formula (6) is replaced with a phosphorus atom (P). Specific examples of such phosphonium cations include tetraalkylphosphonium ions, tetraethylphosphonium ions, tetrapropylphosphonium ions, tetrabutylphosphonium ions, trimethylethylphosphonium ions, triethylmethylphosphonium ions, tetraalkylphosphonium ions, tetraphenyl Examples thereof include tetraarylphosphonium ions such as phosphonium ions. Two or more of R ^{41 to} R ⁴⁴ may be bonded to each other to form a non-aromatic ring (typically, an aliphatic 5-membered ring or 6-membered ring containing phosphorus). .

The salt of any one of the above organic cations (Y ⁺ ) and the anion [ ⁻ N (CORf ¹ ) (SO ₂ Rf ² )] is a salt (room temperature melt) in which at least a part thereof is liquid in the room temperature range. Salt, room temperature molten salt, ionic liquid, etc.). In a preferred embodiment of the amide salt disclosed herein, the melting point of the amide salt is about 30 ° C. or lower (more preferably about 20 ° C. or lower, more preferably about 0 ° C. or lower). Maintain at least a part (preferably all) in a liquid state (molten state) in a temperature range of at least about 20 to 40 ° C. (more preferably about 0 to 60 ° C., more preferably about −20 to + 80 ° C.). Preferred amide salts are preferred.
The anion constituting the amide salt of the present invention includes (1) a sulfonyl group and a carbonyl group bonded to one nitrogen atom, and (2) a perfluoro group bonded to the sulfonyl group and carbonyl group, respectively. And (3). It is characterized in that the perfluoro group (Rf ¹ ) bonded to the carbonyl group has a perfluoroalkyl ether chain. A salt having such an anion can have a lower melting point than a salt having an anion that does not satisfy one or more of the above characteristics (1) to (3). Moreover, it can become a lower viscosity thing. In addition, the ion conductivity can be higher (or a practically preferable ion conductivity can be exhibited even in a lower temperature range). Such an amide salt can be useful as a component of a power storage element and other various electrochemical devices. For example, it can be suitably used as a constituent component of an electrolyte that shows a liquid state in a normal temperature range (for example, an electrolyte for various storage elements such as a lithium ion secondary battery). In such an electrolyte, the amide salt can be preferably used as a solvent (medium) for dissolving the supporting electrolyte.

[Inorganic cation]
In addition, the cation (Y ⁺ ) constituting the amide salt disclosed herein may be an inorganic cation other than a hydrogen ion. Typically, it may be an alkali metal ion such as lithium ion, sodium ion, potassium ion, rubidium ion, or cesium ion. For example, it may be an ion of an alkali metal other than lithium. Other examples of inorganic cations that can be selected as Y ⁺ include ammonium ion (NH ₄ ⁺ ), hydroxyammonium ion (HONH ₃ ⁺ ), hydroxonium ion (H ₃ O ⁺ ), and the like .
The salt of such an inorganic cation (Y ⁺ ) and the above anion [ ⁻ N (CORf ¹ ) (SO ₂ Rf ² )] is, for example, a constituent of an electrolyte described later (typically, an inorganic cation in the electrolyte). Can be suitably used as a supporting electrolyte). In addition, such an amide salt having an inorganic cation is useful as a raw material (intermediate) for producing the amide salt in which Y ⁺ is an organic cation (hereinafter sometimes referred to as “amide organic salt”). obtain. As the amide salt used for the production of the amide organic salt, those in which Y ⁺ is an alkali metal ion (for example, Li ⁺ , Na ⁺ and K ⁺ ) are preferable. For example, an amide metal salt in which Y ⁺ is Na ⁺ or K ⁺ (particularly preferably Na ⁺ ) can be preferably used.

<Method for producing amide salt>
[Method 1]
Any of the amide salts described above is, for example, a step of reacting an acid anhydride represented by the above formula (11) with a sulfonamide salt represented by the above formula (12) (hereinafter referred to as “step A”). And the like can be suitably produced by a production method including As the acid anhydride and sulfonamide salt used in the method, an appropriate compound may be selected according to the structure of the target amide salt (that is, the amide salt represented by the formula (10)). This method can be applied to both the production of an amide salt in which Y ⁺ is an organic cation and the production of an amide salt in which Y ⁺ is an inorganic cation. It can be preferably applied to the production of an amide salt in which Y ⁺ is an inorganic cation (for example, a metal cation such as an alkali metal ion). For example, it is suitable as a method for producing an amide salt in which Y ⁺ is lithium ion (Li ⁺ ), sodium ion (Na ⁺ ), or potassium ion (K ⁺ ).
The acid anhydride used in this method can be easily synthesized by a known method. Alternatively, it is available, for example, from Exfluor Research Corp. (Texas, USA). The sulfonamide salt used in the above method is a known substance that is readily available, or can be easily synthesized by a known method.
Although a solvent is not necessarily required for the above reaction, it is usually preferable to use a solvent because the reaction can proceed more smoothly and with good yield. Solvents used include ethers such as diethyl ether, ethyl propyl ether, dipropyl ether, diisopropyl ether and dibutyl ether; nitriles such as acetonitrile and propionitrile; ketones such as acetone and methyl ethyl ketone; methyl acetate and ethyl acetate One or two or more selected from esters such as methyl propionate; halocarbons such as dichloromethane, trichloromethane, tetrachloromethane, and dichloroethane; For example, ethers can be preferably used.
This reaction can be allowed to proceed in a temperature range of, for example, −30 ° C. to + 100 ° C. From the viewpoint of improving the yield, etc., it is usually preferable to carry out the reaction in a temperature range of 0 ° C. to + 50 ° C.

[Method 2]
In addition, the amide salt represented by the above formula (13) is, for example, a step of reacting an acid halide represented by the above formula (14) with a silylsulfonamide salt represented by the above formula (15) (hereinafter referred to as the following). , Sometimes referred to as “step B”). As the acid halide and silylsulfonamide salt used in the method, an appropriate compound may be selected according to the structure of the target amide salt. This method can be preferably applied to the production of an amide salt in which Y _M ⁺ is an alkali metal ion. For example, it is suitable as a method for producing an amide salt in which Y _M ⁺ is Li ⁺ , Na ⁺ or K ⁺ .
The acid halide used in this method is a known substance that is readily available, or can be easily synthesized by a known method. For example, an acid halide in which X in formula (14) is fluorine (F) or chlorine (Cl) can be preferably used. More preferred are acid halides wherein X is fluorine. The silylsulfonamide salt used in this method is a known substance that is readily available, or can be easily synthesized by a known method. Preference is given to silylsulfonamide salts in which R ⁴ in formula (15) is each a methyl group or an ethyl group. For example, a salt of trimethylsilylsulfonamide and an alkali metal can be preferably used.
Although a solvent is not necessarily required for the above reaction, it is usually preferable to use a solvent because the reaction can proceed more smoothly and with good yield. As the solvent to be used, one or two or more selected from nitriles, ethers, ketones, esters, halocarbons and the like as described above can be appropriately selected. For example, nitriles such as acetonitrile and propionitrile can be preferably used.
This reaction can be allowed to proceed in a temperature range of 0 ° C. to + 150 ° C., for example. From the viewpoint of improving the yield, etc., it is usually preferable to carry out the reaction in a temperature range from room temperature to + 100 ° C.

[Method 3]
In addition, any of the amide salts described above may be referred to as, for example, a step of reacting the amide represented by the above formula (17) with the compound represented by the above formula (18) (hereinafter referred to as “step C”). It can be suitably manufactured by a manufacturing method including. As the amide represented by the formula (17) and the compound represented by the formula (18), an appropriate compound can be used depending on the structure of the target amide salt (that is, the amide salt represented by the formula (16)). Just choose. This method can be applied to both the production of an amide salt in which Y ⁺ is an organic cation and the production of an amide salt in which Y ⁺ is an inorganic cation. It can be preferably applied to the production of an amide salt in which Y ⁺ is an inorganic cation (for example, a metal cation such as an alkali metal ion). For example, it is suitable as a method for producing an amide salt in which Y ⁺ is Li ⁺ , Na ⁺ or K ⁺ .
The amide used in this method (that is, the amide represented by the formula (17)) can be produced by the amide production method disclosed by this specification. The amide production method will be described in detail later. In addition, the compound represented by the formula (18) is a known substance that is readily available, or can be easily synthesized by a known method. A in formula (18) can be a substituted (eg, halogen substituted) or unsubstituted alkyl group, a hydroxy group, or an —O ⁻ Y ⁺ group. A compound in which A is an —O ⁻ Y ⁺ group (ie, carbonate) and a compound in which A is a hydroxy group (ie, bicarbonate) can be preferably used. It is more preferable to use a carbonate represented by the following formula: Y ₂ CO ₃ ;
Although a solvent is not necessarily required for the above reaction, it is usually preferable to use a solvent because the reaction can proceed more smoothly and with good yield. Solvents used include ethers such as diethyl ether, ethyl propyl ether, dipropyl ether, diisopropyl ether and dibutyl ether; nitriles such as acetonitrile and propionitrile; esters such as methyl acetate, ethyl acetate and methyl propionate Ketones such as acetone and methyl ethyl ketone; halocarbons such as dichloromethane, trichloromethane, tetrachloromethane, and dichloroethane; alcohols such as methanol, ethanol, propanol, isopropanol, and t-butanol; one kind selected from water and the like; Two or more kinds can be appropriately selected. The alcohols include halogen-substituted alcohols having a structure in which some or all of hydrogen atoms other than hydroxy groups are replaced with halogen atoms. Preferred solvents include 1,1,1,3,3,3-hexafluoropropan-2-ol [(CF ₃ ) ₂ CHOH], 2,2,2-trifluoroethanol, 2,2,3,3, Examples thereof include one or more selected from halogen-substituted alcohols such as 3-pentafluoropropanol and 2,2,3,3-tetrafluoropropanol, esters, nitriles, and halocarbons.
This reaction can be allowed to proceed in a temperature range of 0 ° C. to + 100 ° C., for example. From the viewpoint of improving the yield, etc., it is usually preferable to carry out the reaction in a temperature range of 0 ° C. to + 50 ° C.

[Method 4]
The amide salt represented by the formula (19) includes, for example, an amide salt (amide metal salt) represented by the formula (20) and a compound (organic salt) represented by the formula (21). Can be suitably manufactured by a manufacturing method including a step of reacting (hereinafter also referred to as “step D”). An appropriate compound may be selected as the amide metal salt represented by the formula (20) and the organic salt represented by the formula (21) according to the structure of the target amide salt. This method can be preferably applied to the production of an amide salt in which Y 2 _O ⁺ is any one of the organic cations described above. For example, it is suitable as a method for producing an amide salt in which Y 2 _O ⁺ is any organic cation represented by the above formulas (3) to (7) and (9).
The amide salt used in this method (that is, the amide metal salt represented by the formula (20)) can be produced by the method disclosed by this specification. For example, an amide metal salt produced by a method including at least one of Step A, Step B, and Step C can be preferably used. It is preferable to use an amide metal salt in which Y _M ⁺ is an alkali metal ion (for example, Li ⁺ , Na ⁺ or K ⁺ ). Further, the organic salt represented by the formula (21) is a known substance that is readily available, or can be easily synthesized by a known method.
Equation (21) in the ^- B may be an inorganic anion, or an organic anion. Examples of such inorganic anions include halogen anions (for example, anions selected from the group consisting of F ⁻ , Cl ⁻ , Br ⁻ and I ⁻ ), BF ₄ ⁻ , PF ₆ ⁻ , AsF ₆ ⁻ , SbF ₆ ⁻ and BCl _4. ^-, SbCl ₅ F ^- can be exemplified such as ^- and SbCl _6. Further, preferred examples of the organic anions may comprise a compound represented by formula ^{_{(21), - OCOCH 3, - OCOC 2}} H 5, - OCOCCl 3, - OSO 2 Ph (Ph represents a phenyl group.) , ^- OSO ₂ Tol (Tol is, o-, represents a m- or p- tolyl ^{_{group.), - OSO 2 C 6}} H 4 NO 2 (C 6 H 4 NO 2 is, o-, m- or p- represents a nitrophenyl ^{_{group), -. OSO 2 C 6}} H 4 Br (C 6 H 4 Br is, o-, represents a m- or p- bromophenyl group), HSO ₄ ^{-., and,} - OSO ₂ OCH ₃ etc. can be illustrated. As the organic anions, ^{further, -} OCORf ^2, - can be exemplified OSO ₂ Rf ² and the like. Here, Rf ² is a group in which all hydrogen atoms of a monovalent organic group containing or not containing an ether bond are replaced with fluorine atoms. For example, Rf ² is a perfluoroalkyl group (—CF ₃ , —C ₂ F _5, etc. ). And Rf ² in these organic anions, and Rf ² in the amide salt represented by the formula (19) may be different may be the same. As the compound represented by the formula (21), for example, a salt of a halogen anion and an organic cation (Y 2 _O ⁺ ), or the above organic anion having the same Rf ² as the amide salt represented by the formula (19) it can be preferably used a salt of ^- (OSO ^₂ Rf _2, etc.) and an organic cation _{(Y O} ^+).
Although a solvent is not necessarily required for the above reaction, it is usually preferable to use a solvent because the reaction can proceed more smoothly and with good yield. As the solvent to be used, one or two or more selected from the above-mentioned nitriles, esters, ketones, halocarbons, alcohols (including halogen-substituted alcohols), water and the like can be appropriately selected. From the viewpoint of economy and / or product purity, water can be preferably selected as the solvent.
This reaction can be allowed to proceed in a temperature range of 0 ° C. to + 100 ° C., for example. From the viewpoint of improving the yield, etc., it is usually preferable to carry out the reaction in a temperature range of 0 ° C. to + 50 ° C.

[Method 5]
The organic cation (Y 2 _O ⁺ ) constituting the amide salt represented by the above formula (19) has a structure in which at least one hydrogen atom is bonded to a nitrogen atom (N), a sulfur atom (S) or a phosphorus atom (P). Of cations. Examples of such organic cations include R ¹¹ or R ¹³ in formula (3), R ²¹ in formula (4), R ³² in formula (5), R ^{41 to} R in formula (6). Examples include a cation having a structure in which any one of ⁴⁴ or any one of R ^{51 to} R ⁵³ in formula (9) is a hydrogen atom (H). The amide salt having an organic cation having such a structure is a mixture of an organic compound corresponding to the conjugate base of the cation and an amide represented by the formula (17) (for example, an amide having an approximately equimolar amount with respect to the compound). Can also be produced.

<Method for producing amide>
[Method 6]
The amide represented by the above formula (17), (22) or (24) is, for example, a step of reacting an amide salt represented by the above formula (25) with an acid (hereinafter also referred to as “step E”). Can be suitably manufactured by a manufacturing method including: As the amide salt represented by the formula (25), an appropriate compound may be selected according to the structure of the target amide. Y ⁺ in formula (25) may be an inorganic cation or an organic cation. In one preferred embodiment of the method disclosed herein, an amide salt wherein Y ⁺ is an inorganic cation is used. For example, an amide metal salt in which Y ⁺ is an alkali metal ion (for example, Li ⁺ , Na ⁺ or K ⁺ ) can be preferably used. In another preferred embodiment, an amide salt in which Y ⁺ is an organic cation (for example, an organic cation represented by the above formula (3) to (7) or (9)) is used. An amide salt in which Y ⁺ is an organic cation represented by the above formula (6) can be preferably used. A preferred example of such an organic cation is a tetraalkylammonium ion. For example, it is preferable to use an amide salt having an ammonium ion in which R ^{41 to} R ⁴⁴ in formula (6) are each independently an alkyl group having 1 to 4 carbon atoms.
The amide salt used in this method (that is, the amide salt represented by the formula (25)) can be produced by the method disclosed by this specification. For example, an amide salt produced by a method including at least one of the above steps A to D can be preferably used. As the acid to be reacted with the amide salt, either an inorganic acid or an organic acid can be used. Usually, it is preferable to use an inorganic acid. Moreover, so-called strong acid can be preferably used. Preferable examples of the acid used in this method include sulfuric acid, chlorosulfuric acid, fluorosulfuric acid, trifluoromethanesulfonic acid and the like. It is particularly preferable to use sulfuric acid from the viewpoints of economy and handling properties.
In the above reaction, an acid can also serve as a solvent. Further, a solvent may be used in order to reduce the amount of acid used or to obtain a product with higher purity when a large excess of acid causes a partial decomposition reaction. As the solvent to be used, the above-described halocarbons are preferable, and dichloromethane, trichloromethane and the like can be preferably used.
This reaction can be allowed to proceed in a temperature range of 0 ° C. to + 150 ° C., for example. From the viewpoints of economy, yield, etc., it is usually preferable to carry out the reaction in a temperature range of 0 ° C to + 120 ° C. For example, the reaction can be performed in a temperature range of room temperature to 100 ° C.

<Method for producing amide salt or amide>
The various amides and amide salts disclosed herein can be suitably produced by a method including one or more of Steps A to E above. For example, any of the following manufacturing methods can be employed.
(1) By performing the above-mentioned Step A or Step B, an amide salt [Y _M ⁺ -N (CORf ¹ ) (SO ₂ Rf ² )] whose cation component is a metal cation (for example, alkali metal ion) is obtained. Step D is performed using the amide metal salt. In this way, an amide salt [Y _O ⁺ -N (CORf ¹ ) (SO ₂ Rf ² )] whose cation component is an organic cation is obtained.
(2) By performing the above-mentioned Step A or Step B, an amide salt [Y _M ⁺ -N (CORf ¹ ) (SO ₂ Rf ² )] whose cation component is a metal cation (for example, alkali metal ion) is obtained. Step E is performed using the amide metal salt. In this way, amide [NH (CORf ¹ ) (SO ₂ Rf ² )] is obtained.
(3) Prepare the amide obtained by (2) above. Step C is performed using the amide and a metal carbonate (eg, alkali metal carbonate) or bicarbonate. In this way, an amide salt [Y _M ⁺ -N (CORf ¹ ) (SO ₂ Rf ² )] whose cation component is a metal cation is obtained.
(4) Prepare the amide metal salt [Y _M ⁺ -N (CORf ¹ ) (SO ₂ Rf ² )] obtained in (3) above. Step D is performed using the amide metal salt. In this way, an amide salt [Y _O ⁺ -N (CORf ¹ ) (SO ₂ Rf ² )] whose cation component is an organic cation is obtained.

Among the amide salts disclosed herein, those in which the cation component Y ⁺ is an organic cation (amide organic salt) may be a salt having a melting point of about 40 ° C. or less. For example, it may be a salt having a melting point of about 30 ° C. or lower (preferably about 20 ° C. or lower, more preferably about 0 ° C. or lower). In a more preferred embodiment, the salt may have a melting point of about −20 ° C. or less (particularly preferably about −30 ° C. or less). The amide salt in which Y ⁺ is an organic cation may be an amide salt that is liquid in the normal temperature range (normal temperature molten salt). For example, it may be an amide organic salt that can maintain a liquid state in a temperature range of at least 10 ° C. to 30 ° C. (more preferably 0 ° C. to 40 ° C., more preferably −20 ° C. to + 60 ° C.).

<Ion conductive material>
A composition containing one or more of the above-mentioned amide salts (that is, an amide salt represented by Y ⁺ -N (CORf ¹ ) (SO ₂ Rf ² )) has a normal temperature range (for example, 10 ° C. to 30 ° C. , Preferably 0 ° C. to 40 ° C., more preferably −20 ° C. to + 60 ° C.). In one preferred embodiment of such a material, the material contains at least ^{one of the} amide organic salts [Y 2 _O ⁺ -N (CORf ¹ ) (SO ₂ Rf ² )] that is liquid in the temperature range. The ion conductive material disclosed herein contains at least one of the above amide salts in which Y ⁺ is an inorganic cation (for example, an alkali metal ion) instead of or in addition to the amide organic salt. can do.
Such ion-conducting material can contain other salts in addition to any of the amide salts described above. Examples of the “other salt” include salts of various inorganic anions with various organic cations or inorganic cations, salts of various organic anions having no perfluoroalkyl ether chain with various organic cations or inorganic cations, and the like. be able to. For example, a salt other than the amide salt, which is liquid in the normal temperature range (normal temperature molten salt) can be contained.
In one preferable embodiment of the ion conductive material disclosed herein, the material is in a liquid state in the normal temperature range in a state of substantially not containing a component (for example, an organic solvent) other than the amide salt. Alternatively, it is in a liquid state in the temperature range in a state in which components other than the amide salt and the other salts are substantially not contained (that is, in a state containing substantially only an ion-binding compound). Such an ion conductive material can be suitable as an electrolyte used for power storage elements such as various batteries and capacitors, or as a component thereof. For example, an ionic conductive material substantially composed of one or more of the above amide organic salts [Y _O ⁺ -N (CORf ¹ ) (SO ₂ Rf ² )] that is liquid at room temperature may be an electricity storage element or the like. In the electrolyte used in the present invention, it can be preferably used as a medium (electrolyte medium (solvent)) for dissolving the supporting electrolyte instead of or together with the conventionally known non-aqueous solvent or the like. In addition, a composition substantially composed of such an amide organic salt and another room temperature molten salt can also be preferably used as an electrolyte medium or the like.

<Electrolyte and battery including the electrolyte>
[Electrolytes]
The ionic conductive composition containing at least one kind of amide organic salt [Y 2 _O ⁺ -N (CORf ¹ ) (SO ₂ Rf ² )] that exhibits a liquid state in a normal temperature range includes, for example, a cation between a positive electrode and a negative electrode. Can be preferably used as an electrolyte or a constituent component of a battery that is charged / discharged when the battery goes back and forth. For example, it is suitable as an electrolyte or a constituent component of a battery (typically a lithium ion secondary battery) in which the cation is lithium ion. In addition to the amide organic salt, the electrolyte used in such a battery can contain a compound (lithium source) that can supply lithium ions to the electrolyte. Examples of such a compound (also referred to as “supporting electrolyte” or “supporting salt”) include LiPF ₆ , LiBF ₄ , LiPF ₅ (CF ₃ ), LiPF ₄ (CF ₃ ) ₂ , LiPF ₄ (CF ₂ CF ₃ ). ₂ , LiBF ₃ (CF ₃ ), LiBF ₂ (CF ₃ ) ₂ , LiBF (CF ₃ ) ₃ , LiBF ₃ (C ₂ F ₅ ), LiAsF ₆ , LiClO ₄ , LiSCN, LiOCOCF ₃ , LiCF ₃ SO ₃ , LiC ₄ F ₉ SO ₃ , LiN (SO ₂ C ₂ F ₅ ) ₂ , LiC (CF ₃ SO ₂ ) ₃ , LiOCOC ₆ F ₅ , LiN (SO ₂ CF ₃ ) ₂ (sometimes expressed as “LiTFSI”) ), LiN (COCF ₃ ) (SO ₂ CF ₃ ), LiN (COCF ₂ CF ₃ ) (SO ₂ CF ₃ ), and other lithium salts can be selected. Electrolytes disclosed herein, in addition to the amide organic salts described above, the following ^{formula: - N (CORf 1) (} SO 2 Rf 2); anion salts of lithium ion represented by may contain . That is, the electrolyte disclosed here may have a composition containing a lithium salt (supporting electrolyte) represented by the following formula: LiN (CORf ¹ ) (SO ₂ Rf ² ); The anion component constituting the lithium salt and the anion component constituting the amide organic salt may be the same or different. For example, it can be set as the electrolyte containing the salt of the same anion component and lithium ion which comprise the amide organic salt. Such an electrolyte is preferable from the viewpoint of, for example, recoverability after use. In one preferred embodiment of the electrolyte disclosed herein, a lithium salt as a supporting electrolyte is dissolved in a liquid medium substantially composed of the amide organic salt that is liquid at around room temperature. In another preferred embodiment of the electrolyte disclosed herein, the lithium salt as the supporting electrolyte is substantially composed of the amide organic salt that is liquid at about room temperature and a room temperature molten salt other than the amide organic salt. It is dissolved in a liquid medium.
The concentration of the supporting electrolyte is not particularly limited. For example, it can be set as the composition which contains about 0.1-20 mol support electrolyte (lithium salt) per liter (L) of electrolyte. Usually, the content of the supporting electrolyte is suitably in the range of 0.3 to 15 mol / L, and preferably in the range of 0.5 to 10 mol / L. In a temperature range of at least 10 ° C. or higher (preferably 0 ° C. or higher), the concentration is preferably set to a level at which the supporting electrolyte can be stably dissolved (precipitation is not observed).

The electrolyte can contain a general solvent (typically an organic solvent). Solvents preferably used include carbonates such as propylene carbonate (PC), ethylene carbonate (EC), dimethyl carbonate, diethyl carbonate (DEC), and ethyl methyl carbonate; cyclic esters such as γ-butyrolactone; methyl acetate and acetic acid Esters such as ethyl, methyl formate and ethyl formate; cyclic ethers such as tetrahydrofuran and 1,3-dioxolane; ethers such as ethylene glycol dimethyl ether, ethylene glycol diethyl ether and diethylene glycol dimethyl ether; Examples thereof include aprotic solvents used for the electrolyte solution of the secondary battery. Moreover, 3,3,4,4-tetrafluorotetrahydrofuran, trifluoropropylene carbonate, CF ₃ COOCH ₃ , C ₂ F ₅ COOCH ₃ , C ₃ F ₇ COOCH ₃ , CF ₃ COOCF ₂ CF ₂ H, CF ₃ COOCH ₂ CF ₃ , CF ₃ COOCH ₂ CF ₂ CF ₂ H, C ₃ F ₇ OCH ₃ , C ₄ F ₉ OCH ₃ , CF ₃ CFHCF ₂ OCH ₂ CF ₃ , C ₃ F ₇ OCF (CF ₃ ) COOCH ₃ , F [ CF (CF ₃ ) CF ₂ O] ₃ CF (CF ₃ ) COOCH _3, F [CF (CF ₃ ) CF ₂ O] ₃ CF (CF ₃ ) COOCH ₃ or the like containing at least one fluorine atom in the molecule Solvent (fluorine organic solvent): trimethyl phosphate, triethyl phosphate, ethyl dimethyl phosphate, diethyl methyl phosphate, tripropyl phosphate Phosphate esters containing or not containing fluorine atoms such as phosphate, tributyl phosphate, tri (trifluoromethyl) phosphate, tri (trifluoroethyl) phosphate, tri (perfluoroethyl) phosphate; be able to. These solvents are preferred because they are nonflammable or flame retardant. One or more selected from the above-described solvents and the like can be contained in the electrolyte.
Although not particularly limited, in an electrolyte containing such a solvent, the content ratio of the solvent can be made equal to or less than the content ratio of the amide organic salt. That is, the content of the solvent can be 50 parts by mass or less (preferably 25 parts by mass or less, more preferably 10 parts by mass or less) with respect to 50 parts by mass of the amide organic salt constituting the electrolyte. Thus, an electrolyte containing an amide organic salt as a main component is a preferred example of the electrolyte disclosed herein.

  The electrolyte disclosed here can be made of a composition consisting essentially of an ion-binding compound (salt). For example, it may be a composition substantially composed of one or more of the amide organic salts and a supporting electrolyte (for example, a lithium salt). You may further contain normal temperature molten salts other than the said amide organic salt. A liquid electrolyte having such a composition and having a normal temperature range (for example, 10 ° C. to 30 ° C., preferably 0 ° C. to 40 ° C., more preferably −20 ° C. to + 60 ° C.) is preferable. An electrolyte that can maintain a liquid state even at about −30 ° C. is particularly preferable. A lithium ion secondary battery including such an electrolyte can be suitably used in a temperature range of, for example, −30 ° C. or higher (typically −30 ° C. to + 100 ° C.). In particular, it can be a lithium ion secondary battery exhibiting improved characteristics (such as ionic conductivity) in a temperature range of room temperature or lower (more preferably 0 ° C. or lower).

[Other battery components]
A battery including the electrolyte as described above may include a positive electrode having an active material capable of reversibly inserting and extracting lithium ions (for example, insertion and extraction). As such an active material for a positive electrode, various lithium composite oxides containing lithium and a transition metal as constituent elements can be preferably used. Examples of such complex oxides include Li—Ni oxides, Li—Mn oxides, Li—Co oxides, and the like. Here, “Li—Ni-containing oxide” means an oxide having Li and Ni as constituent elements, and at least one other metal element other than Li and Ni (that is, a transition metal element other than Li and Ni) And / or an oxide containing a typical metal element). The metal element is a kind selected from the group consisting of Co, Al, Mn, Cr, Fe, V, Mg, Ti, Zr, Nb, Mo, W, Cu, Zn, Ga, In, Sn, La, and Ce. Or it can be two or more. The same applies to the Li—Mn-containing oxide and the Li—Co-containing oxide.

  The positive electrode of the battery disclosed herein may have a configuration in which the positive electrode active material as described above is held on a conductive member. As the conductive member (current collector), a rod-like body, a plate-like body, a foil-like body, a net-like body or the like mainly composed of a metal such as aluminum (Al), nickel (Ni), titanium (Ti), or the like is used. be able to. Alternatively, carbon paper or the like may be used. For example, it can be set as the structure which provided the layer (active material content layer) containing an active material in the surface of a sheet-like electroconductive member (for example, Al foil). In addition to the active material, the active material-containing layer can contain one or more materials used for a general positive electrode as necessary. Examples of such materials include conductive materials and binders. As the conductive material, one or more selected from carbon materials such as carbon black (acetylene black and the like), conductive metal powders such as nickel powder, and the like can be used. As the binder, polyvinylidene fluoride (PVDF), polytetrafluoroethylene (PTFE), polyvinylidene fluoride-hexafluoropropylene copolymer (PVDF-HFP), styrene butadiene block copolymer (SBR), carboxymethyl cellulose ( One or more selected from CMC) and the like can be used.

The battery disclosed herein can include a negative electrode having an active material capable of reversibly inserting and extracting lithium ions (for example, insertion and extraction). As the negative electrode active material, a carbon material having an amorphous structure and / or a graphite structure can be used. For example, natural graphite, mesocarbon microbeads (MCMB), highly oriented graphite (HOPG), hard carbon, soft carbon, etc., one or more active materials used for the negative electrode of general lithium ion secondary batteries Can be preferably used. Alternatively, oxide, chalcogenide, or the like can be used. For example, lithium titanate (for example, Li ₄ Ti ₆ O ₁₂ ) can be preferably used as the negative electrode active material. Such an active material can be made into a negative electrode having a configuration in which a conductive member made of metal or the like is held together with a binder or the like as necessary. As the conductive member (current collector), a rod-like body, a plate-like body, a foil-like body, a net-like body mainly composed of a metal such as copper (Cu), aluminum (Al), nickel (Ni), titanium (Ti), etc. Etc. can be used. Alternatively, carbon paper or the like may be used. As the binder, the same as the positive electrode can be used. For example, it can be set as the structure which provided the layer (active material content layer) containing an active material in the surface of a sheet-like electroconductive member (for example, Cu foil).

The battery disclosed here can be configured such that the electrolyte is disposed between the positive electrode and the negative electrode. Further, a separator may be disposed between the positive electrode and the negative electrode, and an electrolyte may be infiltrated into the separator. As the separator, for example, a porous film made of a polyolefin resin such as polyethylene (PE) or polypropylene (PP) can be used. Moreover, you may use the woven fabric or nonwoven fabric which consists of a polypropylene, a polyethylene terephthalate (PET), methylcellulose (MC) etc.
Examples of the electrolyte disclosed herein include polyethylene oxide (PEO), ethylene oxide-propylene oxide copolymer (EO-PO), polymethyl methacrylate (PMMA), polyvinylidene fluoride (PVdF), and polyvinylidene fluoride-hexafluoro. It can be used as a solid electrolyte by molding (film formation) together with a support such as a propylene copolymer (PVdF-HFP).

  Examples of the present invention will be described below, but the present invention is not intended to be limited to the specific examples.

上記式（Ｓ１）に示す合成スキームに沿って、下記表１に示す反応条件により、パーフルオロアルキルエーテル基を有する非対称アミドのナトリウム塩を合成した。
すなわち、反応容器にトリフルオロメタンスルホンアミドナトリウム塩（化合物１）２０１ｍｍｏｌと乾燥ジエチルエーテル１００ｍＬとを入れて氷浴で冷却した。この溶液中に、Exfluor Research Corp.社（Texas, U.S.A.）から入手可能な２−（トリフルオロメトキシ）ジフルオロ酢酸無水物（化合物２）２６１ｍｍｏｌを乾燥ジエチルエーテル１００ｍＬに溶解させた溶液を、３５分かけて滴下した。滴下終了後、氷浴を外して室温でさらに４時間攪拌した。その後、アスピレータを用いて溶媒を留去し、さらに１１０℃で真空乾燥させた。このようにして、Ｎ−（トリフルオロメタンスルホニル）−２−（トリフルオロメトキシ）ジフルオロアセトアミドナトリウム塩［ＮａＮ（ＣＯＣＦ₂ＯＣＦ₂）（ＳＯ₂ＣＦ₃）］１９７ｍｍｏｌを得た。収率は９８％であった。 <Synthesis of amide metal salt>
[Synthesis Example 1]

According to the synthesis scheme shown in the above formula (S1), a sodium salt of an asymmetric amide having a perfluoroalkyl ether group was synthesized under the reaction conditions shown in Table 1 below.
That is, 201 mmol of trifluoromethanesulfonamide sodium salt (Compound 1) and 100 mL of dry diethyl ether were placed in a reaction vessel and cooled in an ice bath. In this solution, 261 mmol of 2- (trifluoromethoxy) difluoroacetic anhydride (Compound 2) available from Exfluor Research Corp. (Texas, USA) was dissolved in 100 mL of dry diethyl ether over 35 minutes. And dripped. After completion of dropping, the ice bath was removed and the mixture was further stirred at room temperature for 4 hours. Then, the solvent was distilled off using an aspirator, and further vacuum dried at 110 ° C. In this way, 197 mmol of N- (trifluoromethanesulfonyl) -2- (trifluoromethoxy) difluoroacetamide sodium salt [NaN (COCF ₂ OCF ₂ ) (SO ₂ CF ₃ )] was obtained. The yield was 98%.

[Synthesis Examples 2 to 5]
Using each amide metal salt (compound 1) and acid anhydride (compound 2) shown in Table 1, reaction and post-treatment in the same manner as in Synthesis Example 1 with the solvents and reaction conditions shown in the same table (evaporation and drying of the solvent) By performing the above, each product shown in Table 1 was obtained. Table 1 also shows the yield of the product.
The acid anhydrides [(CF ₃ CF ₂ OCF ₂ CO) ₂ O, (CF ₃ OCF ₂ CF ₂ CO) ₂ O, and (CF ₃ OCF ₂ CF ₂ OCF ₂ CO)] used in Synthesis Examples 2 to 5 ₂ O] is available from Exfluor Research Corp.

[Synthesis Example 6]
A sodium salt of an asymmetric amide having a perfluoroalkyl ether group was synthesized as follows.
That is, 62.6 mmol of silylsulfonamide sodium salt (Compound 1) shown in Table 1 and acetonitrile were placed in a reaction vessel. A solution prepared by dissolving 75.3 mmol of oxyfluoride (compound 2) shown in Table 1 in acetonitrile was dropped into this solution at room temperature and stirred for 30 minutes, and then the system was heated to 80 ° C. and further heated. Stir for 61 hours. Then, the post-process was performed like the synthesis example 1 and the amide salt shown in Table 1 was obtained (yield 95%). The acid fluoride is available from, for example, SynQuest Labs (Florida, USA).

上記式（Ｓ２）に示す合成スキームに沿って、下記表２に示す反応条件により、パーフルオロアルキルエーテル基を有する非対称アミドのリチウム塩を合成した。
すなわち、容量１００ｍＬのナス型フラスコに炭酸リチウム（化合物２）０．５５５ｇ（７．５ｍｍｏｌ）およびジエチルエーテル ２０ｍＬを入れて氷浴で冷却した。この溶液中に、Ｎ−（トリフルオロメタンスルホニル）−２−（トリフルオロメトキシ）−ジフルオロアセトアミド（化合物１）４．６７ｇ（１５ｍｍｏｌ）をジエチルエーテル４０ｍＬに溶解させた溶液を滴下して１０分間攪拌した後、氷浴を外して室温でさらに２時間攪拌した。その後、溶媒を留去し、真空減圧下において１５０℃で３時間乾燥させた。このようにして、Ｎ−（トリフルオロメタンスルホニル）−２−（トリフルオロメトキシ）−ジフルオロアセトアミドリチウム塩（生成物）４．６２ｇを得た。収率は９７％であった。この生成物は、常温においてガラス状の固体であった。 [Synthesis Example 7]

A lithium salt of an asymmetric amide having a perfluoroalkyl ether group was synthesized under the reaction conditions shown in Table 2 below in accordance with the synthesis scheme shown in the above formula (S2).
That is, 0.555 g (7.5 mmol) of lithium carbonate (Compound 2) and 20 mL of diethyl ether were placed in a 100 mL capacity eggplant type flask and cooled in an ice bath. In this solution, a solution prepared by dissolving 4.67 g (15 mmol) of N- (trifluoromethanesulfonyl) -2- (trifluoromethoxy) -difluoroacetamide (Compound 1) in 40 mL of diethyl ether was added dropwise and stirred for 10 minutes. Thereafter, the ice bath was removed and the mixture was further stirred at room temperature for 2 hours. Thereafter, the solvent was distilled off, followed by drying at 150 ° C. for 3 hours under vacuum. In this way, 4.62 g of N- (trifluoromethanesulfonyl) -2- (trifluoromethoxy) -difluoroacetamido lithium salt (product) was obtained. The yield was 97%. This product was a glassy solid at room temperature.

[Synthesis Example 8]
This synthesis example is an example in which the same amide salt as synthesis example 7 was synthesized by changing the reaction solvent.
That is, as shown in Table 2, 2.5 mmol of lithium carbonate (compound 2) and 1,1,1,3,3,3-hexafluoropropan-2-ol [(CF ₃ ) ₂ as a solvent in a reaction vessel. CHOH] 2.5 mL was added, and a solution prepared by dissolving 5.1 mmol of the amide (Compound 1) shown in Table 2 in 2.5 mL of (CF ₃ ) ₂ CHOH was added dropwise at room temperature and stirred for 2 hours. Then, the post-process was performed like the synthesis example 7, and the product was obtained. The yield was 97%.
Compound 1 used in Synthesis Examples 7 and 8 was obtained in Synthesis Example 55 described later.

[Synthesis Examples 9 to 17]
These amides (compound 1) and alkali metal carbonates (compounds 2) shown in Tables 2 to 3 were used and reacted and worked up in the same manner as in Synthesis Example 8 with the solvents and reaction conditions shown in the same table. Each product shown in the table was obtained. The yield of each product is also shown in the table.
In addition, the compound 1 used by these synthesis examples is obtained by either of the synthesis examples 55-59 mentioned later, respectively. The product of Synthesis Example 9 is the same amide salt as the product of Synthesis Example 1. Similarly, the product of Synthesis Example 11 is the synthesis example 2 and the synthesis example 13 is the synthesis example 3. The product of Example 14 is the same amide salt as that of Synthesis Example 5, the product of Synthesis Example 15 is the same as that of Synthesis Example 4, and the product of Synthesis Example 17 is the same as the product of Synthesis Example 6.

<Physical properties and analysis results of the obtained amide salt>
Melting | fusing point of each product obtained by the synthesis examples 1-17 was measured by the conventional method. In addition, elemental analysis of each product was performed, and it was confirmed that the calculated value and the analytical value were almost the same. Further, each product was dissolved in acetonitrile-d _3, and ¹⁹ F-NMR spectrum was measured using C ₆ F ₆ as a standard. The obtained data is shown in Table 4.
In addition, about each product obtained by the synthesis examples 7, 8, 10, 12, 14, 16, and 17, the above measurement and analysis were performed after further purifying these products. That is, a small amount (0.05 mol%) of an amide corresponding to the conjugate acid of each product (amide metal salt) was added to a solution in which each product was dissolved in an appropriate amount of solvent [(CF ₃ ) ₂ CHOH] at room temperature. And stirred. After the solvent was distilled off, the residue was dried at 150 ° C. under vacuum for 3 hours to obtain a high purity amide salt. The amide salt was used for the above measurement and analysis.
In addition, since the products obtained by Synthesis Examples 9, 11, 13, 14, 15 and 17 were higher in purity than the products obtained by Synthesis Examples 1 to 6, Table 4 Shows the data obtained for the products of Synthesis Examples 9, 11, 13, 14, 15 and 17.

上記式（Ｓ３）に示す合成スキームに沿って、下記表５に示す反応条件により、パーフルオロアルキルエーテル基を有する非対称アミドのイミダゾリウム塩を合成した。
すなわち、反応容器に１，３−ジメチルイミダゾリウム トリフルオロメタンスルホナート（トリフラートともいう。表中では「^-ＯＴｆ」と示すこともある。）（化合物１）１０ｍｍｏｌと水５ｍＬとを入れた。これを攪拌しながら、合成例９（または合成例１）により得られたＮａＮ（ＣＯＣＦ₂ＯＣＦ₂）（ＳＯ₂ＣＦ₃）（化合物２）１０．５ｍｍｏｌを水５ｍＬに溶解させた溶液を加え、室温で１０分間攪拌した。その後、下層である油層を分離し、これを水で繰り返し洗浄した。得られた油状物を、真空ポンプを用いた減圧下において１１０℃で３時間乾燥させた。このようにして、１，３−ジメチルイミダゾリウム Ｎ−（トリフルオロメタンスルホニル）−２−（トリフルオロメトキシ）ジフルオロアセトアミド ６．２ｍｍｏｌを得た。収率は６２％であった。 <Synthesis of amide salt having imidazolium cation>
[Synthesis Example 18]

According to the synthesis scheme shown in the above formula (S3), an imidazolium salt of an asymmetric amide having a perfluoroalkyl ether group was synthesized under the reaction conditions shown in Table 5 below.
That is, (also referred to as triflate in the table.. A ^"- OTf" and sometimes shown) into the reaction vessel, 3-dimethyl imidazolium trifluoromethanesulfonate (compound 1) was placed and 10mmol of water 5 mL. While stirring this, a solution prepared by dissolving 10.5 mmol of NaN (COCF ₂ OCF ₂ ) (SO ₂ CF ₃ ) (Compound 2) obtained in Synthesis Example 9 (or Synthesis Example 1) in 5 mL of water was added, Stir at room temperature for 10 minutes. Thereafter, the lower oil layer was separated and repeatedly washed with water. The resulting oil was dried at 110 ° C. for 3 hours under reduced pressure using a vacuum pump. In this way, 6.2 mmol of 1,3-dimethylimidazolium N- (trifluoromethanesulfonyl) -2- (trifluoromethoxy) difluoroacetamide was obtained. The yield was 62%.

[Synthesis Examples 19 to 35]
Using each imidazolium salt (Compound 1) shown in Tables 5 to 9 and an asymmetric amide metal salt having a perfluoroalkyl ether group (Compound 2), in the same manner as in Synthesis Example 18 with the solvents and reaction conditions shown in the same table Each product shown in these tables was obtained by carrying out the reaction and post-treatment. The yield of each product is also shown in the table. In addition, as the compound 2 in these synthesis examples, the amide salt obtained by any of the synthesis examples 9, 11, 13, 15, and 17 (or synthesis examples 1-4 and 6) was used, respectively.

<Synthesis of amide salt having pyridinium cation>
[Synthesis Example 36]
Using the pyridinium salt (Compound 1) shown in Table 9 and the amide salt (Compound 2) obtained in Synthesis Example 9 (or Synthesis Example 1), in the same manner as in Synthesis Example 18 with the solvents and reaction conditions shown in the same table By carrying out the reaction and post-treatment, the products shown in the same table were obtained. The yield was 66%.

<Synthesis of amide salt having oxazolium cation>
[Synthesis Example 37]
Using the oxazolium salt (Compound 1) shown in Table 9 and the amide salt (Compound 2) obtained in Synthesis Example 9, the reaction and post-treatment are performed in the same manner as in Synthesis Example 18 with the solvents and reaction conditions shown in the same table. As a result, products shown in the same table were obtained. The yield was 54%.

The melting points of the products obtained in Synthesis Examples 18 to 37 were all below normal temperature (about 20 ° C. here). In addition, elemental analysis of each product was performed, and it was confirmed that the calculated value and the analytical value were almost the same. Further, the ¹⁹ F-NMR spectrum of each product was measured in the same manner as described above. Further, each product was dissolved in acetonitrile-d ₃ and a ¹ H-NMR spectrum was measured. The obtained data are shown in Tables 10-11.

<Synthesis of amide salt having tetraalkylammonium cation>
[Synthesis Example 38]
Using an ammonium salt (Compound 1) shown in Table 12 and an amide salt (Compound 2) obtained by Synthesis Example 9 (or Synthesis Example 1), an asymmetric amide anion having a perfluoroalkyl ether group and a tetraalkylammonium cation A salt with was synthesized.
That is, 15 mmol of tetramethylammonium chloride (Compound 1) and water were placed in a reaction vessel. While stirring this, an aqueous solution of 15.8 mmol of NaN (COCF ₂ OCF ₂ ) (SO ₂ CF ₃ ) (Compound 2) was added and stirred at room temperature for 20 minutes. Thereafter, post-treatment was performed in the same manner as in Synthesis Example 18 to obtain tetramethylammonium N- (trifluoromethanesulfonyl) -2- (trifluoromethoxy) difluoroacetamide. The yield was 53%.

[Synthesis Examples 39 to 43]
Using each ammonium salt shown in Table 12 (compound 1) and a metal salt of an asymmetric amide having a perfluoroalkyl ether group (compound 2), the reaction and Each product shown in these tables was obtained by post-treatment. The yield of each product is also shown in the table. In addition, as the compound 2 in these synthesis examples, the amide salt obtained by any of the synthesis examples 9, 11, 13, 15, and 17 (or synthesis examples 1-4 and 6) was used, respectively.

The melting points of the products obtained in Synthesis Examples 38 to 43 were all below normal temperature (about 20 ° C. here). In addition, elemental analysis of each product was performed, and it was confirmed that the calculated value and the analytical value were almost the same. Further, ¹⁹ F-NMR spectrum and ¹ H-NMR spectrum of each product were measured in the same manner as described above. Table 13 shows the obtained data.

<Synthesis of amide salt having aliphatic cyclic ammonium cation>
[Synthesis Example 44]
A salt of an asymmetric amide anion having a perfluoroalkyl ether group and an aliphatic cyclic ammonium cation was synthesized as follows.
That is, an aliphatic cyclic ammonium salt (Compound 1) and water shown in Table 14 were placed in a reaction vessel. While stirring this, an aqueous solution of 15.8 mmol of the amide salt (Compound 2) obtained in Synthesis Example 9 (or Synthesis Example 1) was added and stirred at room temperature for 10 minutes. Then, the post-process was performed similarly to the synthesis example 18, and the product shown in the same table was obtained. The yield was 56%.

[Synthesis Examples 45 to 48]
Using each aliphatic cyclic ammonium salt (Compound 1) shown in Table 14 and the amide salt (Compound 2) obtained in Synthesis Example 9 (or Synthesis Example 1), the synthesis examples were carried out using the solvents and reaction conditions shown in the same table. Each product shown in these tables was obtained by carrying out the reaction and post-treatment in the same manner as in 44. The yield of each product is also shown in the table.

The melting points of the products obtained in Synthesis Examples 44 to 48 were all below normal temperature (about 20 ° C. here). In addition, elemental analysis of each product was performed, and it was confirmed that the calculated value and the analytical value were almost the same. Further, ¹⁹ F-NMR spectrum and ¹ H-NMR spectrum of each product were measured in the same manner as described above. Table 15 shows the obtained data.

[Synthesis Example 49]
A salt of an asymmetric amide anion having a perfluoroalkyl ether group and an aliphatic cyclic ammonium cation having an alkyl ether group was synthesized as follows.
That is, 50 mmol of an aliphatic cyclic ammonium salt (Compound 1) shown in Table 16 and water were placed in a reaction vessel. While stirring this, an aqueous solution of 52.5 mmol of the amide salt (Compound 2) obtained in Synthesis Example 9 (or Synthesis Example 1) was added, and the mixture was stirred at room temperature for 20 minutes. Then, the post-process was performed similarly to the synthesis example 18, and the product shown in the same table was obtained. The yield was 61%.

[Synthesis Examples 50 to 52]
Using each aliphatic cyclic ammonium salt shown in Table 16 (Compound 1) and a metal salt of an asymmetric amide having a perfluoroalkyl ether group (Compound 2), the same as in Synthesis Example 49 with the solvents and reaction conditions shown in the same table The products shown in these tables were obtained by reaction and post-treatment. The yield of each product is also shown in the table. As compound 2 in these synthesis examples, an amide salt obtained in any one of synthesis example 9 (or synthesis example 1) and synthesis example 13 (or synthesis example 3) was used, respectively.

The melting points of the products obtained in Synthesis Examples 49 to 52 were all below normal temperature (about 20 ° C. here). In addition, elemental analysis of each product was performed, and it was confirmed that the calculated value and the analytical value were almost the same. Further, ¹⁹ F-NMR spectrum and ¹ H-NMR spectrum of each product were measured in the same manner as described above. Table 17 shows the obtained data.

<Synthesis of amide salt having sulfonium cation>
[Synthesis Example 53]
A sulfonium salt of an asymmetric amide anion having a perfluoroalkyl ether group was synthesized as follows.
That is, 15 mmol of sulfonium salt (Compound 1) shown in Table 18 and water were placed in a reaction vessel. While stirring this, an aqueous solution of 15.8 mmol of the amide salt (Compound 2) obtained in Synthesis Example 9 (or Synthesis Example 1) was added, and the mixture was stirred at room temperature for 20 minutes. Then, the post-process was performed similarly to the synthesis example 18, and the product shown in the same table was obtained. The yield was 39%.
The melting point of the product obtained in Synthesis Example 53 was not more than room temperature (about 20 ° C. here). In addition, elemental analysis of this product was performed, and it was confirmed that the calculated value and the analytical value were almost the same. In addition, the ¹⁹ F-NMR spectrum and ¹ H-NMR spectrum of the product were measured in the same manner as described above. The obtained data is shown in Table 19.

上記式（Ｓ４）に示す合成スキームに沿って、パーフルオロアルキルエーテル基を有する非対称アミドを合成した。
すなわち、蒸留物受け容器と連結された蒸留塔を取り付けた５０ｍＬのナス型フラスコに、ＮａＮ（ＣＯＣＦ₂ＯＣＦ₂）（ＳＯ₂ＣＦ₃）１１．６６ｇ（３５ｍｍｏｌ）と硫酸７．６ｍＬ（１０５ｍｍｏｌ）とを入れた。蒸留物受け容器を−４０℃に冷却した後、真空ポンプにより系を減圧にし、上記ナス型フラスコ（反応容器）を油浴に浸け、内容物を攪拌しつつ油浴の温度を４０℃まで上昇させた。さらに油浴の温度を８０℃まで徐々に上げた。このようにして蒸留物受け容器内に目的物（生成物）を、ガラス状固体として得た。収量は１０．８３ｇ、収率は９９．５％であった。なお、上記化合物１としては、合成例１により得られたアミド塩を使用した。 <Synthesis of amide>
[Synthesis Example 54]

According to the synthesis scheme shown in the above formula (S4), an asymmetric amide having a perfluoroalkyl ether group was synthesized.
That is, in a 50 mL eggplant type flask equipped with a distillation column connected to a distillate receiving vessel, 11.66 g (35 mmol) of NaN (COCF ₂ OCF ₂ ) (SO ₂ CF ₃ ) and 7.6 mL (105 mmol) of sulfuric acid were added. Put. After cooling the distillate receiving container to −40 ° C., the system is depressurized by a vacuum pump, the eggplant type flask (reaction container) is immersed in an oil bath, and the temperature of the oil bath is increased to 40 ° C. while stirring the contents. I let you. Further, the temperature of the oil bath was gradually increased to 80 ° C. Thus, the target product (product) was obtained as a glassy solid in the distillate receiving container. The yield was 10.83 g and the yield was 99.5%. As the compound 1, the amide salt obtained in Synthesis Example 1 was used.

上記式（Ｓ５）に示す合成スキームに沿って、下記表２０に示す反応条件により、パーフルオロアルキルエーテル基を有する非対称アミドを合成した。
すなわち、３００ｍＬの丸底フラスコに、化合物１としてのＮ−（トリフルオロメタンスルホニル）−２−（トリフルオロメトキシ）ジフルオロアセトアミドのテトラエチルアンモニウム塩１１．０ｇ（２５ｍｍｏｌ）と、溶媒としてのジクロロメタン２５０ｍＬとを入れて室温で攪拌した。これに硫酸１２．５ｍＬ（２３５ｍｍｏｌ）を加えて３０分間攪拌した後、上層のジクロロメタン層を分離した。残った下層をさらにジクロロメタン２５ｍＬで抽出した。この抽出操作を三回繰り返した。抽出液を集めて溶媒を留去し、残渣を減圧蒸留し、沸点８６〜８７℃／２８ｍｍＨｇの留分を集めた。この留分（生成物）の収量は６．０２ｇ、収率は７７％であった。なお、化合物１としては、合成例３９により得られたアミド塩を使用した。 [Synthesis Example 55]

Asymmetric amides having a perfluoroalkyl ether group were synthesized according to the reaction conditions shown in Table 20 below along the synthesis scheme shown in the above formula (S5).
That is, 11.0 g (25 mmol) of tetraethylammonium salt of N- (trifluoromethanesulfonyl) -2- (trifluoromethoxy) difluoroacetamide as Compound 1 and 250 mL of dichloromethane as a solvent were placed in a 300 mL round bottom flask. And stirred at room temperature. To this was added 12.5 mL (235 mmol) of sulfuric acid and stirred for 30 minutes, and then the upper dichloromethane layer was separated. The remaining lower layer was further extracted with 25 mL of dichloromethane. This extraction operation was repeated three times. The extract was collected, the solvent was distilled off, and the residue was distilled under reduced pressure to collect a fraction having a boiling point of 86 to 87 ° C./28 mmHg. The yield of this fraction (product) was 6.02 g, and the yield was 77%. As compound 1, the amide salt obtained in Synthesis Example 39 was used.

[Synthesis Examples 56 to 59]
Using each amide salt (compound 1) and acid shown in Table 20 and the reaction and post-treatment in the same manner as in Synthesis Example 55 using the solvents and reaction conditions shown in the same table, the products shown in these tables are obtained. It was. The yield of each product is also shown in the table. In addition, as the compound 1 in these synthesis examples, the amide salt obtained by any of the synthesis examples 40-43 was used, respectively.

Elemental analysis of each product (target product) obtained in Synthesis Examples 54 to 59 was performed, and it was confirmed that the calculated value and the analyzed value were almost consistent. Further, ¹⁹ F-NMR spectrum and ¹ H-NMR spectrum of each product were measured in the same manner as described above. The obtained data are shown in Table 21 together with the boiling points (distillation conditions) of the respective products.

<Measurement of ionic conductivity>
The ionic conductivity of some salts obtained by the synthesis examples described above was measured. The measurement is performed using the model name “Model 3100” manufactured by YSI, and as a probe using the product name “3417” manufactured by YSI, the product name “MI-915” or “MI-905” manufactured by MicroElectrodes, and an argon atmosphere. Went under.

Samples 1 to 4 shown in Table 22 are examples in which the ionic conductivity at the measurement temperatures of 20 ° C., 0 ° C., −20 ° C. and −30 ° C. was measured by the above method for the salts of cations and anions shown in the same table. . These salts are salts of 1,3-dimethylimidazolium cation and various asymmetric amide anions having a perfluoroalkyl group containing an ether bond, respectively, according to each synthesis example shown in parentheses in the table. The obtained salt. In the table, as samples 5 and 6, the same imidazolium cation and bis (trifluoromethanesulfonyl) imide anion salt as in samples 1 to 4 (sample 5), and the cation and 2,2,2-trifluoro The ionic conductivity of the salt with N- (trifluoromethanesulfonyl) acetamide (sample 6) is also shown. The salt of sample 5 was solid at any of the measurement temperatures described above, and the salt of sample 6 was solid at a measurement temperature of 0 ° C. or lower. Thus, a sample that is solid at the measurement temperature has substantially no ionic conductivity compared to a liquid sample. Therefore, the ion conductivity when the sample is solid at the measurement temperature is indicated as “˜0”.
As can be seen from Table 22, the salts of Samples 1 to 4 clearly had better low-temperature characteristics (for example, ionic conductivity in a temperature range of 0 ° C. or lower) than the salts of Samples 5 and 6. Therefore, a battery using the salt of Samples 1 to 4 as an electrolyte or a component thereof functions appropriately in a wider temperature range (particularly a low temperature range) than a battery using the salt of Samples 5 and 6. obtain.

Sample 7 shown in Table 23 is a salt of 1,2,3,4-tetramethylimidazolium cation and an asymmetric amide anion having a perfluoroalkyl ether group. As Sample 7, the amide salt obtained in Synthesis Example 30 was used. Sample 8 shown in the same table is a salt of the imidazolium cation and 2,2,3,3,3-pentafluoro-N- (trifluoromethanesulfonyl) propionamide. For these samples, the ion conductivity at a measurement temperature of 20 ° C. was measured in the same manner as described above.
As can be seen from Table 23, the salt of Sample 7 exhibited better ionic conductivity than the salt of Sample 8 having different types of anions.

Samples 9 and 10 shown in Table 24 are salts of each pentaalkylimidazolium cation shown in the same table and an asymmetric amide anion having a perfluoroalkyl ether group. As Sample 9, the amide salt obtained in Synthesis Example 34 was used, and as Sample 10, the amide salt obtained in Synthesis Example 35 was used. Samples 11 and 12 shown in the same table are salts different from the sample 9 in the type of anion. For these samples, the ionic conductivity at a measurement temperature of 20 ° C. was measured in the same manner as described above. The results obtained are shown in Table 24. The table also shows the ionic conductivity of Sample 13, which is a salt having a different anion type from Sample 10. This is cited from the data described on pages 256-257 (issued in October 2002) of the 42nd Battery Discussion Meeting 1B09. Note that the salts of Samples 11 and 12 were both solid at the measurement temperature.
As can be seen from Table 24, both the salts of Samples 9 and 10 clearly showed better ionic conductivity than the salts of Samples 11-13.

Samples 14 to 16 shown in Table 25 are salts of each aliphatic cyclic ammonium cation and an asymmetric amide anion having a perfluoroalkyl ether group shown in the same table. The amide salt obtained in Synthesis Example 45 was used as Sample 14, the amide salt obtained in Synthesis Example 49 was used as Sample 15, and the amide salt obtained in Synthesis Example 52 was used as Sample 16. For these samples, the ion conductivity at a measurement temperature of 20 ° C. was measured in the same manner as described above. The results obtained are shown in Table 24. The table also shows the ionic conductivity of Sample 17, which is a salt of an aliphatic cyclic ammonium cation and TFSI. This is cited from the data described in J. Phys. Chem. B, Vol. 103, No. 2, pp. 4164-4170 (1999).
As can be seen from Table 25, the salts of Samples 14 to 16 all showed better ionic conductivity than the salt of Sample 17.

<Measurement of potential width>
The electrochemical stability of Samples 18-20 shown in Table 26 was evaluated. Here, the sample 18 is a perfluoroalkyl ether to a 1,2,3,4-tetramethylimidazolium salt of an asymmetric amide having a perfluoroalkyl ether group (the salt obtained in Synthesis Example 30 was used). It is a composition prepared by dissolving a lithium salt of an asymmetric amide having a group (the salt obtained in Synthesis Example 8 was used) at a concentration of 12 mol%. Sample 19 is a composition prepared by dissolving LiTFSI at a concentration of 11 mol% in the imidazolium salt. Sample 20 is a composition prepared by dissolving a lithium salt of 2,2,2-trifluoro-N- (trifluoromethanesulfonyl) acetamide at a concentration of 7 mol% in the imidazolium salt. All of these compositions were liquid at 20 ° C.
The electrochemical stability of these samples was evaluated as follows. That is, a three-electrode electrochemical cell was constructed using each sample as an electrolyte, a glassy carbon electrode as a working electrode, lithium metal as a counter electrode, and lithium metal as a reference electrode. The cell thus prepared was subjected to linear sweep voltammetry measurement at room temperature (about 23 ° C.) under the condition of a sweep rate of 10 mV / sec. The same shall apply hereinafter) and the oxidation potential was examined. The results are shown in Table 26. Further, the width of the potential window (potential width) obtained from the difference between the oxidation potential and the reduction potential is shown in the same table.
As can be seen from Table 26, the compositions of Samples 18 to 20 in which various lithium salts were dissolved in the imidazolium salt obtained in Synthesis Example 30 were all -0.2 to 0.1 V (that is, 0.5 V). Hereinafter, the reduction potential was as low as 0.3 V or less. All of these compositions exhibited high oxidation potentials of 5.2 to 5.6 V (that is, 5 V or more). For this reason, all of these compositions have a wide potential width of 5 V or more. In particular, the composition of Sample 18 in which the lithium salt of Synthesis Example 8 is dissolved in the imidazolium salt of Synthesis Example 30 exhibits a particularly low reduction potential (−0.2 V) and a particularly high oxidation potential (5.6 V). For this reason, it has a particularly wide potential width (5.8 V).

Further, the electrochemical stability of the salts of Sample 21 and Sample 22 shown in Table 26 was evaluated in the same manner as Samples 18-20. That is, an electrochemical cell was constructed in the same manner as described above except that these samples were used as electrolytes. As the sample 21, the salt obtained in Synthesis Example 50 was used. As Sample 22, as shown in Table 26, a salt having a different anion type from Sample 21 was used. By performing linear sweep voltammetry measurement on these cells in the same manner as described above, the reduction potential (to lithium metal, the same applies hereinafter) and the oxidation potential of each salt were examined. The results are shown in Table 26. The width of the potential window obtained from the difference between the oxidation potential and the reduction potential is shown in the same table.
As can be seen from Table 26, the salt of Sample 21 exhibited a low reduction potential of −0.1 V (ie, 0 V or less) and a high oxidation potential of 5.4 V (ie, 5 V or more). For this reason, this salt had a wide potential width of 5.5V. In addition, the salt of sample 21 had a lower reduction potential than the salt of sample 22, and thus the potential window was wider.

Specific examples of the present invention have been described in detail above, but these are merely examples and do not limit the scope of the claims. The technology described in the claims includes various modifications and changes of the specific examples illustrated above.
In addition, the technical elements described in the present specification or the drawings exhibit technical usefulness alone or in various combinations, and are not limited to the combinations described in the claims at the time of filing. In addition, the technology illustrated in the present specification or the drawings achieves a plurality of objects at the same time, and has technical utility by achieving one of the objects.

Claims (19)

Following formula (1):

(Rf ¹ is a group in which all hydrogen atoms of a monovalent organic group having an alkyl chain containing an ether bond in at least a part of its chemical structure are replaced by fluorine atoms. Rf ² contains an ether bond or A group in which all hydrogen atoms of a monovalent organic group not included are replaced with fluorine atoms, Y ⁺ is a cation other than hydrogen ions);
An amide salt represented by 2. The amide salt according to claim 1, wherein Rf ¹ in the formula (1) is a C 2-10 perfluoroalkyl group containing an ether bond. Rf ¹ in the formula (1) is the following formula (2):
^{-Rf 3 -O (-Rf 4 -O)} n -Rf 5 (2)
(Rf ³ and Rf ⁴ are each independently a perfluoroalkylene group having 1 to 3 carbon atoms. Rf ⁵ is a perfluoroalkyl group having 1 to ⁵ carbon atoms. N is 0 to 2);
The amide salt of Claim 2 represented by these. In the formula (2), Rf ³ and Rf ⁴ are each independently a perfluoroalkylene group having 1 or 2 carbon atoms, Rf ⁵ is a perfluoroalkyl group having 1 to 3 carbon atoms, and n is 0 or 1 The amide salt according to claim 3, wherein Rf ² in the formula (1) is a perfluoroalkyl group having 1 to 5 carbon atoms, amide salt according to any one of claims 1 to 4. The amide salt according to any one of claims 1 to 5, wherein Y ⁺ in the formula (1) is an alkali metal cation. The amide salt according to any one of claims 1 to 5, wherein Y ⁺ in the formula (1) is an organic cation.   The amide salt according to claim 7, which is liquid in a normal temperature range.   An electrolyte containing the amide salt according to claim 7.   A lithium ion secondary battery comprising the electrolyte according to claim 9. Following formula (10):

(Rf ¹ is a group in which all hydrogen atoms of a monovalent organic group having an alkyl chain containing an ether bond in at least a part of its chemical structure are replaced with fluorine atoms. Rf ² contains an ether bond or A group in which all hydrogen atoms of a monovalent organic group not included are replaced with fluorine atoms, Y ⁺ is a cation other than hydrogen ions);
A process for producing an amide salt represented by:
Following formula (11):
(Rf ¹ CO) ₂ O (11)
(Rf ¹ is the same as Rf ¹ in formula (10).);
An acid anhydride represented by
Following formula (12):
_{^{Y + - NH (SO 2 Rf}} 2) (12)
(Y ⁺ and Rf ² are the same as Y ⁺ and Rf ^{2 in} formula (10), respectively);
An amide salt production method of reacting with a sulfonamide salt represented by the formula: Following formula (13):

(Rf ¹ is a group in which all hydrogen atoms of a monovalent organic group having an alkyl chain containing an ether bond in at least a part of its chemical structure are replaced by fluorine atoms. Rf ² contains an ether bond or A group in which all hydrogen atoms of a monovalent organic group not included are replaced by fluorine atoms, Y _M ⁺ is a metal cation.);
A process for producing an amide salt represented by:
Following formula (14):
Rf ¹ COX (14)
(Rf ¹ is the same as Rf ¹ in formula (13). X is a halogen atom);
An acid halide represented by
Following formula (15):
_{^{Y M + - N (Si (}} R 4) 3) (SO 2 Rf 2) (15)
(Y _M ⁺ and Rf ² are the same as Y _M ⁺ and Rf ^{2 in} Formula (13), respectively. R ⁴ is independently an alkyl group having 1 to 4 carbon atoms);
An amide salt production method of reacting with a silylsulfonamide salt represented by the formula: Following formula (16):

(Rf ¹ is a group in which all hydrogen atoms of a monovalent organic group having an alkyl chain containing an ether bond in at least a part of its chemical structure are replaced with fluorine atoms. Rf ² contains an ether bond or A group in which all hydrogen atoms of a monovalent organic group not included are replaced with fluorine atoms, Y ⁺ is a cation other than hydrogen ions);
A process for producing an amide salt represented by:
Following formula (17):

(Rf ¹ and Rf ² are the same as Rf ¹ and Rf ^{2 in} formula (16), respectively);
An amide represented by
Following formula (18):
Y ^{+ -} OCOA (18)
(A is a substituted or unsubstituted alkyl group, hydroxy group or -O, ^- a is .Y ⁺ is Y ⁺ groups are the same as Y ⁺ in the formula (16).)
A method for producing an amide salt, wherein the compound represented by the formula is reacted. The method according to claim 13, wherein Y ⁺ in the formula (16) is an alkali metal cation.   The method according to claim 13 or 14, wherein the salt represented by the formula (18) is a carbonate and / or a bicarbonate. Following formula (19):

(Rf ¹ is a group in which all hydrogen atoms of a monovalent organic group having an alkyl chain containing an ether bond in at least a part of its chemical structure are replaced with fluorine atoms. Rf ² contains an ether bond or (This is a group in which all hydrogen atoms of a monovalent organic group not included are replaced with fluorine atoms. Y 2 _O ⁺ is an organic cation.)
A process for producing an amide salt represented by:
Following formula (20):

(Rf ¹ and Rf ² are the same as Rf ¹ and Rf ^{2 in} formula (19), respectively. Y _M ⁺ is a metal cation.);
An amide salt represented by
Following formula (21):
Y _O ^{+ -} B (21)
; ^- _{(Y O} ⁺ is the same as _{Y O} ⁺ in the formula (19) B is the anion of an inorganic or organic..)
A method for producing an amide salt, wherein the compound represented by the formula is reacted. Following formula (22):

(Rf ¹ is a group in which all hydrogen atoms of a monovalent organic group having an alkyl chain containing an ether bond in at least a part of its chemical structure are replaced with fluorine atoms. Rf ² contains an ether bond or This is a group in which all hydrogen atoms of a monovalent organic group not included are replaced with fluorine atoms.);
An amide represented by Following formula (24):

(Rf ¹ is a group in which all hydrogen atoms of a monovalent organic group having an alkyl chain containing an ether bond in at least a part of its chemical structure are replaced by fluorine atoms. Rf ² contains an ether bond or This is a group in which all hydrogen atoms of a monovalent organic group not included are replaced with fluorine atoms.);
A process for producing an amide represented by:
Following formula (25):

(Rf ¹ and Rf ² are the same as Rf ¹ and Rf ^{2 in} formula (24), respectively. Y ⁺ is a cation other than a hydrogen ion);
An amide production method in which an amide salt represented by formula (I) is reacted with an acid.   The method of claim 18, wherein the acid is sulfuric acid.