JPWO2016039274A1 - Modified rubber and method for producing the same, rubber composition, and tire - Google Patents

Abstract

The present invention provides a compound represented by formula (1) or formula (2). (Wherein X is an acid forming a salt with the guanidine moiety, and R1 and R2 are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl group, And an alkenyl group (all of these groups include those having one or more substituents containing a sulfur atom, a nitrogen atom, or an oxygen atom), and a hydrogen atom. (In the formula, R 1 and R 2 are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl group, and an alkenyl group (all of these groups are a sulfur atom, a nitrogen atom) Including those having one or more substituents containing an atom or oxygen atom), and at least one selected from the group consisting of hydrogen atoms.)

Description

  The present invention relates to a novel bisalkylidene diaminoguanidine and a salt thereof, a modified rubber, a rubber composition, and a tire.

  Aminoguanidine is a synthetic raw material for drugs, dyes, photographic drugs, explosives, and the like, and is widely known to exhibit an anti-glycation action in the pharmaceutical field (see, for example, Non-Patent Document 1). The anti-glycation action of aminoguanidine has been confirmed to inhibit the generation of AGEs in vitro, the inhibition of protein cross-linking and polymerization, the prevention of nephropathy, retinopathy and neuropathy in diabetic model animals, and the prevention of diabetic complications. (For example, see Non-Patent Document 2).

  In recent years, aminoguanidine has been found to be used as an absorbent for odor components of aldehydes, that is, as an aldehyde catcher agent in addition to the above uses (see, for example, Patent Document 1) (see Patent Document 1). For example, see Patent Document 2). The physical properties required for such applications are diversifying, and there is a need to provide compounds that replace conventional aminoguanidines.

  The filler used for rubber is a compounding agent used for the purpose of mixing with rubber to reinforce or increase the rubber, or to give a special function to the rubber. Carbon black, which is a typical filler, not only contributes to the improvement (reinforcing effect) of mechanical properties such as the elastic modulus and breaking strength of rubber, but also has a function of imparting conductivity.

  A method of using an inorganic filler such as silica is known as a method for obtaining a rubber composition having a rubber reinforcing effect similar to carbon black and having a low exothermic property, that is, low loss. The method has been applied to a method for producing a rubber composition for a low fuel consumption tire in consideration of environmental performance.

  In a rubber composition containing an inorganic filler, when the inorganic filler is compounded, the inorganic filler, particularly hydrophilic silica having a silanol group on the surface has a low affinity with the hydrophobic rubber, and the rubber composition Aggregates inside. Therefore, it is necessary to increase the affinity between silica and rubber in order to enhance the reinforcement by silica and obtain a low heat generation effect. As the method, synthetic rubber (for example, refer to Patent Document 3) whose affinity with an inorganic filler is improved by terminal modification with a polar group, and a polar group-containing monomer is copolymerized with an inorganic filler. Synthetic rubber with improved affinity (for example, see Patent Document 4) is known. As a method for modifying a natural rubber to introduce a polar group, a method in which the natural rubber is oxidized and then modified with a hydrazide compound having a polar group (see, for example, Patent Document 5), a modified natural rubber having a polar group introduced therein A method for further improving the dispersibility of silica by adding a silane coupling agent to a rubber composition containing silica (for example, see Patent Document 6) is known.

“Guanidine salt”, Fine Chemical, CMC Publishing, June 2008, Vol. 37, No. 6, p. 72-75 Reiko Naito and one other, “Functions and Development of Anti-Glycation Interesting Materials in the Body” Fine Chemical, CMC Publishing, June 2012, Vol. 41, No. 6, p. 21-26

JP 2005-97340 A JP 2010-248334 A JP 2010-209253 A JP 2011-38009 A JP 2009-108204 A JP 2011-246513 A

  In the future, it is expected that there will be an ever-increasing interest in environmental issues such as an increase in atmospheric carbon dioxide concentration and air pollution, which will reduce the rolling resistance of tires and lead to lower fuel consumption of automobiles. There is a need for a technique for providing a rubber composition containing a rubber and an inorganic filler such as silica and having excellent low loss properties, and a tire.

  The present invention has been made in view of the above problems of the prior art, and an object thereof is to provide a novel bisalkylidene diaminoguanidine and a salt thereof useful as a rubber additive or the like.

  As a result of intensive studies, the present inventors have succeeded in producing a novel bisalkylidene diaminoguanidine and a salt thereof, and have completed the present invention.

  That is, the present invention is as follows.

（式中、Ｘは、グアニジン部位と塩を形成している酸であり、Ｒ^１及びＲ^２は、それぞれ独立して、炭素数１〜１８のアルキル基、シクロアルキル基、アリール基、アルキルアリール基、及びアルケニル基（これらの基は、いずれも硫黄原子、窒素原子、又は酸素原子を含む置換基を１つ以上有するものを含む）、並びに水素原子からなる群より選択される少なくとも１種である。）

（式中、Ｒ^１及びＲ^２は、それぞれ独立して、炭素数１〜１８のアルキル基、シクロアルキル基、アリール基、アルキルアリール基、及びアルケニル基（これらの基は、いずれも硫黄原子、窒素原子、又は酸素原子を含む置換基を１つ以上有するものを含む）、並びに水素原子からなる群より選択される少なくとも１種である。）
［２］
式（３）で表される化合物及び式（４）で表される化合物を反応させて得られる、［１］に記載の化合物。

（式中、Ｘは、式（３）のグアニジン部位と塩を形成している酸である。）

（式中、Ｒ^１及びＲ^２は、それぞれ独立して、炭素数１〜１８のアルキル基、シクロアルキル基、アリール基、アルキルアリール基、アルケニル基（これらの基はいずれも硫黄原子、窒素原子、又は酸素原子を含む置換基を１つ以上有するものを含む）及び水素原子からなる群より選択される少なくとも１種である。）
［３］
式（１）又は式（２）に記載のＲ^１及びＲ^２が、それぞれ独立して、炭素数１〜８のアルキル基、アリール基、及びアルケニル基、並びに水素原子からなる群より選択される少なくとも１種である、［１］又は［２］に記載の化合物。
［４］
融点が５０〜３００℃である、［１］〜［３］のいずれかに記載の化合物。
［５］
式（５）〜（１０）、及び（１２）〜（１４）のいずれかで表される、［１］〜［４］のいずれかに記載の化合物。

［６］
天然ゴム及び合成ゴムからなる群より選択される少なくとも１種を、［１］〜［５］のいずれかに記載の化合物によって変性させて得られる、変性ゴム（Ａ）。
［７］
前記天然ゴム及び合成ゴムからなる群より選択される少なくとも１種と前記式（１）又は式（２）で表される化合物とを、２０〜１８０℃の温度下で混合し、変性させて得られる、［６］に記載の変性ゴム（Ａ）。
［８］
前記式（１）又は式（２）で表される化合物の使用量が、天然ゴム及び合成ゴムの総量に対して、０．０１〜１０質量％である、［６］又は［７］に記載の変性ゴム（Ａ）。
［９］
［６］〜［８］のいずれかに記載の変性ゴム（Ａ）、無機充填材（Ｂ）を含む充填材、及びシランカップリング剤（Ｃ）を含有する、ゴム組成物。
［１０］
前記無機充填材（Ｂ）がシリカである、［９］に記載のゴム組成物。
［１１］
前記充填材がカーボンブラックを含む、［９］又は［１０］に記載のゴム組成物。
［１２］
前記式（１）又は式（２）で表される化合物と、前記天然ゴム及び合成ゴムからなる群より選択される少なくとも１種と、前記無機充填材（Ｂ）を含む充填材と、前記シランカップリング剤（Ｃ）とを混合して得られ、
［９］〜［１１］のいずれかに記載の変性ゴム（Ａ）を含有する、ゴム組成物。
［１３］
混合時の温度が、２０〜１８０℃の範囲にある、［１２］に記載のゴム組成物。
［１４］
前記式（１）又は式（２）で表される化合物の使用量が、前記天然ゴム及び前記合成ゴムの総量に対して、０．０１〜１０質量％である、［１２］又は［１３］に記載のゴム組成物。
［１５］
［９］〜［１４］のいずれかに記載のゴム組成物をタイヤ部材のトレッドに用いた、タイヤ。[1]
The compound represented by Formula (1) or Formula (2).

Wherein X is an acid forming a salt with the guanidine moiety, and R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl A group, and an alkenyl group (all of these groups include those having one or more substituents containing a sulfur atom, a nitrogen atom, or an oxygen atom), and at least one selected from the group consisting of hydrogen atoms is there.)

(In the formula, R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl group, and an alkenyl group (all of these groups are sulfur atoms, Including those having one or more substituents containing a nitrogen atom or an oxygen atom), and at least one selected from the group consisting of hydrogen atoms.)
[2]
The compound according to [1], obtained by reacting the compound represented by formula (3) and the compound represented by formula (4).

(In the formula, X is an acid that forms a salt with the guanidine moiety of formula (3).)

(In the formula, R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl group, or an alkenyl group (all of these groups are a sulfur atom, a nitrogen atom) Or one having at least one substituent containing an oxygen atom) and at least one selected from the group consisting of hydrogen atoms.)
[3]
R ¹ and R ² described in Formula (1) or Formula (2) are each independently selected from the group consisting of an alkyl group having 1 to 8 carbon atoms, an aryl group, an alkenyl group, and a hydrogen atom. The compound according to [1] or [2], which is at least one kind.
[4]
The compound according to any one of [1] to [3], which has a melting point of 50 to 300 ° C.
[5]
The compound according to any one of [1] to [4], which is represented by any one of formulas (5) to (10) and (12) to (14).

[6]
Modified rubber (A) obtained by modifying at least one selected from the group consisting of natural rubber and synthetic rubber with the compound according to any one of [1] to [5].
[7]
At least one selected from the group consisting of the natural rubber and the synthetic rubber and the compound represented by the formula (1) or the formula (2) are mixed at a temperature of 20 to 180 ° C. and modified. The modified rubber (A) according to [6].
[8]
The amount of the compound represented by the formula (1) or the formula (2) is 0.01 to 10% by mass with respect to the total amount of natural rubber and synthetic rubber, according to [6] or [7]. Modified rubber (A).
[9]
A rubber composition comprising the modified rubber (A) according to any one of [6] to [8], a filler containing an inorganic filler (B), and a silane coupling agent (C).
[10]
The rubber composition according to [9], wherein the inorganic filler (B) is silica.
[11]
The rubber composition according to [9] or [10], wherein the filler contains carbon black.
[12]
The compound represented by the formula (1) or the formula (2), at least one selected from the group consisting of the natural rubber and the synthetic rubber, a filler containing the inorganic filler (B), and the silane Obtained by mixing with a coupling agent (C),
A rubber composition containing the modified rubber (A) according to any one of [9] to [11].
[13]
The rubber composition according to [12], wherein the temperature during mixing is in the range of 20 to 180 ° C.
[14]
The amount of the compound represented by the formula (1) or the formula (2) is 0.01 to 10% by mass with respect to the total amount of the natural rubber and the synthetic rubber, [12] or [13] The rubber composition as described in 2.
[15]
[9] A tire using the rubber composition according to any one of [14] to a tread of a tire member.

  The bisalkylidene diaminoguanidine and its salt according to the present invention are useful as rubber additives and the like.

  Hereinafter, a mode for carrying out the present invention (hereinafter simply referred to as “the present embodiment”) will be described in detail. The following embodiments are examples for explaining the present invention, and are not intended to limit the present invention to the following contents. The present invention can be implemented with appropriate modifications within the scope of the gist thereof.

（式中、Ｘは、グアニジン部位と塩を形成している酸であり、Ｒ^１及びＲ^２は、それぞれ独立して、炭素数１〜１８のアルキル基、シクロアルキル基、アリール基、アルキルアリール基、及びアルケニル基（これらの基は、いずれも硫黄原子、窒素原子、又は酸素原子を含む置換基を１つ以上有するものを含む）、並びに水素原子からなる群より選択される少なくとも１種である。）

（式中、Ｒ^１及びＲ^２は、それぞれ独立して、炭素数１〜１８のアルキル基、シクロアルキル基、アリール基、アルキルアリール基、及びアルケニル基（これらの基は、いずれも硫黄原子、窒素原子、又は酸素原子を含む置換基を１つ以上有するものを含む）、並びに水素原子からなる群より選択される少なくとも１種である。）<Bisalkylidene diaminoguanidine and its salt>
The compound of the present embodiment is a compound represented by formula (1) or formula (2) (hereinafter referred to as “bisalkylidene diaminoguanidine”, “bisalkylidene diaminoguanidine salt”, or “bisalkylidene diaminoguanidine or a salt thereof”). Say.)

Wherein X is an acid forming a salt with the guanidine moiety, and R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl A group, and an alkenyl group (all of these groups include those having one or more substituents containing a sulfur atom, a nitrogen atom, or an oxygen atom), and at least one selected from the group consisting of hydrogen atoms is there.)

(In the formula, R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl group, and an alkenyl group (all of these groups are sulfur atoms, Including those having one or more substituents containing a nitrogen atom or an oxygen atom), and at least one selected from the group consisting of hydrogen atoms.)

  X in the formula (1) is not particularly limited, and examples thereof include organic acids and inorganic acids. More specifically, hydrochloric acid, sulfuric acid, carbonic acid, nitric acid, acetic acid, oxalic acid, phosphoric acid, p-toluenesulfonic acid , Hydrobromic acid, hydroiodic acid, sulfamic acid, perchloric acid, silicic acid, boric acid, phenylphosphinic acid and the like. Of these, hydrochloric acid, sulfuric acid, carbonic acid, and nitric acid, which are easily commercially available, are preferred, and hydrochloric acid and carbonic acid are more preferred because of the ease of purification during production.

In the compound of this embodiment, in Formula (1) or Formula (2), R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl group, And an alkenyl group (all of these groups include those having one or more substituents containing a sulfur atom, a nitrogen atom, or an oxygen atom), and at least one selected from the group consisting of hydrogen atoms, Among these, at least one selected from the group consisting of an alkyl group having 1 to 8 carbon atoms, an aryl group, an alkenyl group, and a hydrogen atom is preferable.

  Specific examples of such substituents are not particularly limited, but are methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, sec-butyl group, tert-butyl group, pentyl group, 1-methylbutyl. Group, 2-methylbutyl group, 3-methylbutyl group, 1-ethylpropyl group, 2-ethylpropyl group, 1,1-dimethylpropyl group, 1,2-dimethylpropyl group, 2,2-dimethylpropyl group, vinyl group 1-methylvinyl group, 2-methylvinyl group, 1-ethylvinyl group, 2-ethylvinyl group, 1,2-dimethylvinyl group, 1-propylvinyl group, 1-isopropylvinyl group, 1-ethyl-2-methyl Vinyl group, 2-ethyl-1-methylvinyl group, 1-butylvinyl group, 1-sec-butylvinyl group, 1-tert-butylvinyl 1-isobutyl vinyl group, 2-butyl vinyl group, 2-sec-butyl vinyl group, 2-tert-butyl vinyl group, 2-isobutyl vinyl group, 2-methyl-1-propyl vinyl group, 2-methyl-1-isopropyl vinyl Group, 1,2-diethylvinyl group, 1-methyl-2-propylvinyl group, 1-methyl-2-isopropylvinyl group, 2-phenylvinyl group, etc., methyl group, ethyl group, isopropyl group, butyl Group, pentyl group, vinyl group, 1-methylvinyl group, 2-methylvinyl group and 2-phenylvinyl group are preferred.

  Although it does not specifically limit as a specific example of the compound represented by Formula (1) or Formula (2) of this embodiment, Bis ethylidene diamino guanidine (salt), bispropylidenediamino guanidine (salt), bis butylidene diamino Guanidine (salt), bis (2-methylpropylidene) diaminoguanidine (salt) represented by formula (11), bispentylidenediaminoguanidine (salt), bis (2-methylbutylidene) diaminoguanidine (salt), Bis (3-methylbutylidene) diaminoguanidine (salt), bis (2,2-dimethylpropylidene) diaminoguanidine (salt), bishexylidenediaminoguanidine (salt), bis (2-methylpentylidene) diaminoguanidine (Salt), bis (3-methylpentylidene) diaminoguanidine (salt), bis (4-methyl) Nylidene) diaminoguanidine (salt), bis (2,3-dimethylbutylidene) diaminoguanidine (salt), bis (2,2-dimethylbutylidene) diaminoguanidine (salt), bis (3,3-dimethylbutylidene) Diaminoguanidine (salt), bis (1-methylethylidene) diaminoguanidine (salt), bis (1-methylpropylidene) diaminoguanidine (salt) represented by formula (14), bis represented by formula (5) (1,2-dimethylpropylidene) diaminoguanidine (salt), bis (1-methylbutylidene) diaminoguanidine (salt), bis (1,2-dimethylbutylidene) diaminoguanidine (salt), bis (1,3 -Dimethylbutylidene) diaminoguanidine (salt), bis (1-methylpentylidene) diaminoguanidine represented by formula (6) (Salt), bis (1-methylhexylidene) diaminoguanidine (salt), bis (1-ethylpropylidene) diaminoguanidine (salt) represented by formula (7), bis (1-isopropyl-2- Methylpropylidene) diaminoguanidine (salt), bisarylidenediaminoguanidine (salt), bis (1-methylarylidene) diaminoguanidine (salt), bis (1-ethylarylidene) diamino represented by formula (12) Guanidine (salt), bis (1-propylarylidene) diaminoguanidine (salt), bis (2-methylarylidene) diaminoguanidine (salt) represented by formula (8), bis (1,2-dimethylarylidene) ) Diaminoguanidine (salt), bis (2-ethylarylidene) diaminoguanidine (salt), bis (2-propylarylidene) diaminogua Nidin (salt), bis (2-isopropylarylidene) diaminoguanidine (salt), bis (2-butylarylidene) diaminoguanidine (salt), bis (2-isobutylarylidene) diaminoguanidine (salt), bis (2 -Sec-butylarylidene) diaminoguanidine (salt), bis (2-tert-butylarylidene) diaminoguanidine (salt), bis (2- (1-methylbutyl) arylidene) diaminoguanidine (salt), bis (2- (2-Methylbutyl) arylidene) diaminoguanidine (salt), bis (2- (3-methylbutyl) arylidene) diaminoguanidine (salt), bis (2- (1-ethylpropyl) arylidene) diaminoguanidine (salt), bis ( 2- (2-Ethylpropyl) arylidene) diaminoguanidine (salt), bis (2- 1,1-dimethylpropyl) arylidene) diaminoguanidine (salt), bis (2- (2,2-dimethylpropyl) arylidene) diaminoguanidine (salt), bis (3-methylarylidene represented by formula (9) ) Diaminoguanidine (salt), bis (3-ethylarylidene) diaminoguanidine (salt), bis (3-propylarylidene) diaminoguanidine (salt), bis (3-isopropylarylidene) diaminoguanidine (salt), bis (3-butylarylidene) diaminoguanidine (salt), bis (3-isobutylarylidene) diaminoguanidine (salt), bis (3-sec-butylarylidene) diaminoguanidine (salt), bis (3-tert-butyl Arylidene) diaminoguanidine (salt), bis (3- (1-methylbutyl) arylidene) di Minoguanidine (salt), bis (3- (2-methylbutyl) arylidene) diaminoguanidine (salt), bis (3- (3-methylbutyl) arylidene) diaminoguanidine (salt), bis (3- (1,1-dimethyl) Propyl) arylidene) diaminoguanidine (salt), bis (3- (2-ethylpropyl) arylidene) diaminoguanidine (salt), bis (3- (1,2-dimethylpropyl) arylidene) diaminoguanidine (salt), bis ( 3- (2,2-dimethylpropyl) arylidene) diaminoguanidine (salt), bis (3-phenylarylidene) diaminoguanidine (salt), bis (1-methyl) represented by formula (10) and formula (13) -3-phenylarylidene) diaminoguanidine (salt) and the like.

  Among the compounds represented by the above formula (1) or formula (2), compounds other than the compound represented by the following formula (11) are preferable.

Among the compounds represented by the above formula (1) or formula (2), preferred compounds include compounds represented by the following formulas.

（式中、Ｘは、式（３）のグアニジン部位と塩を形成している酸である。）

（式中、Ｒ^１及びＲ^２は、それぞれ独立して、炭素数１〜１８のアルキル基、シクロアルキル基、アリール基、アルキルアリール基、及びアルケニル基（これらの基は、いずれも硫黄原子、窒素原子、又は酸素原子を含む置換基を１つ以上有するものを含む）、並びに水素原子からなる群より選択される少なくとも１種である。）The compound represented by Formula (1) or Formula (2) of this embodiment can be obtained by a known method. For example, the compound represented by Formula (3) (“1,3-diaminoguanidine salt”) , Simply referred to as “guanidine salt”) and a compound represented by formula (4) (also referred to as “carbonyl compound”). Such a manufacturing method is preferable from the viewpoint of manufacturing cost. More specifically, the compound represented by Formula (1) or Formula (2) includes a compound represented by Formula (3) and acetone or methyl ethyl ketone represented by Formula (4) that forms an alkylidene skeleton. And the like in an alcohol solvent such as water or methanol.

(In the formula, X is an acid that forms a salt with the guanidine moiety of formula (3).)

(In the formula, R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl group, and an alkenyl group (all of these groups are sulfur atoms, Including those having one or more substituents containing a nitrogen atom or an oxygen atom), and at least one selected from the group consisting of hydrogen atoms.)

  The compound represented by the formula (1) or formula (2) to be obtained is often a salt represented by the formula (1), but a compound that is not a salt represented by the formula (2) may be obtained. is there. In the case of forming a salt, for example, an acid that forms a salt with the compound represented by the formula (1) can be appropriately selected according to the type of the compound represented by the formula (3) and the acid to be added. .

  The compound represented by Formula (1) or Formula (2) to be obtained is often a salt represented by Formula (1), but depending on the type of compound represented by Formula (4) and production conditions. The acid used with respect to 1 mol of the compound represented by the formula (1) or the formula (2) may be 1 mol or less or may not form a salt with the acid.

  The compound represented by the formula (3) exhibits strong basicity because the positive charge of the conjugate acid is resonance-stabilized by a plurality of nitrogen atoms present in the molecule, and usually a complex with an acid ( Salt). Specific examples of the compound represented by the formula (3) include, but are not limited to, 1,3-diaminoguanidine carbonate, 1,3-diaminoguanidine hydrochloride, 1,3-diaminoguanidine hydroiodide, 1,3-diaminoguanidine sulfate, 1,3-diaminoguanidine nitrate, 1,3-diaminoguanidine oxalate, 1,3-diaminoguanidine phosphate, 1,3-diaminoguanidine acetate, 1,3- Diaminoguanidine sulfamate, 1,3-diaminoguanidine perchlorate, 1,3-diaminoguanidine hydrobromide, 1,3-diaminoguanidine silicate, 1,3-diaminoguanidine borate, 1 , 3-diaminoguanidine phenylphosphinate and the like. Among these, commercially available 1,3-diaminoguanidine hydrochloride, 1,3-diaminoguanidine sulfate, 1,3-diaminoguanidine carbonate, and 1,3-diaminoguanidine nitrate are preferable. Of these, 1,3-diaminoguanidine carbonate and 1,3-diaminoguanidine hydrochloride are preferable.

Examples of the compound represented by the formula (4) is not particularly limited, R ¹ and R ² is an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, alkylaryl group and alkenyl group (these groups, Are compounds having at least one selected from the group consisting of hydrogen atoms, including those having one or more substituents containing a sulfur atom, a nitrogen atom, or an oxygen atom. A compound that is at least one selected from the group consisting of 1 to 8 alkyl groups, aryl groups, and alkenyl groups, and a hydrogen atom is economically available, or can be used in an aqueous solvent. preferable.

  Specific examples of the compound represented by the formula (4) are not particularly limited, but acetone, methyl ethyl ketone, diethyl ketone, methyl isopropyl ketone, methyl isobutyl ketone, methyl tert-butyl ketone, 2-pentanone, 2-hexanone, 2 -Heptanone, formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, isobutyraldehyde, valeraldehyde, isovaleraldehyde, 2-methylbutyraldehyde, pivalaldehyde, acrolein, methacrolein, crotonaldehyde, 2-pentenal, 2-hexenal, 2 -Heptenal, 2-octenal, benzylideneacetone and the like. Among them, acetone, methyl ethyl ketone, diethyl ketone, Le isopropyl ketone, methyl isobutyl ketone, 2-pentanone, 2-hexanone, 2-heptanone, formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, isobutyraldehyde, acrolein, methacrolein, crotonaldehyde, benzylidene acetone is preferred.

  These carbonyl compounds are all known compounds and can also be obtained as commercial products. In addition, there is a compound in which an isomer of a trans isomer and a cis isomer exists such as crotonaldehyde, and any of a mixture of a trans isomer and a cis isomer and a compound of only a trans isomer may be used. .

  The reaction conditions of the compound represented by formula (3) and the compound represented by formula (4) will be described in detail. In the reaction, for example, with respect to 1 mol of the compound represented by the formula (3), the compound represented by the formula (4) is used in an amount of 2.0 mol to excess, and if necessary, an acid catalyst as a condensation accelerator. Use 0.001 to 2.0 mol, preferably 0.01 to 1.0 mol, and stir in a polar solvent such as water or alcohol at normal pressure at 0.0 to 100 ° C. for 10 minutes to 24 hours. It progresses by making it react. After the reaction, the target product may be purified by a known method. For example, there is a method of obtaining crude crystals by cooling with ice water and precipitating and isolating crystals.

  The use ratio of the compound represented by the formula (3) and the compound represented by the formula (4) is a molar ratio, preferably 1.0: 2.0 to 1.0: 100, more preferably 1. 0: 2.0 to 1.0: 10. The reaction may be carried out at room temperature, or may be carried out at a high temperature as necessary. In consideration of the boiling point of the starting carbonyl compound, it is preferably 0.0 to 100 ° C., more preferably about 20 to 80 ° C. Do.

  The atmosphere in which the reaction is performed may be an air atmosphere or an inert gas atmosphere such as nitrogen or argon.

  The reaction pressure is preferably carried out under atmospheric pressure from the economical point of view, but can also be carried out under high pressure or reduced pressure.

  The pH in the reaction system may be neutral, but it is preferable to use the above acid as a condensation accelerator because the reaction proceeds rapidly.

  Although it does not specifically limit as said polar solvent, Water, methanol, ethanol, propanol, isopropyl alcohol, butanol, isobutyl alcohol, etc. are mentioned. Carbonyl compounds as raw materials, that is, acetone, methyl ethyl ketone, diethyl ketone, isopropyl aldehyde, methyl isopropyl ketone, methyl isobutyl ketone, 2-pentanone, 2-hexanone, 2-heptanone, formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, isobutyraldehyde Acrolein, methacrolein, crotonaldehyde, benzylideneacetone and the like can also be used. An aqueous solvent is preferable from the economical aspect.

  The condensation accelerator is not particularly limited, but hydrochloric acid, sulfuric acid, acetic acid, p-toluenesulfonic acid, nitric acid, oxalic acid, phosphoric acid, hydrobromic acid, hydroiodic acid, sulfamic acid, perchloric acid, etc. Is mentioned. It is preferable to use the same acid as that of the diaminoguanidine salt as the raw material.

  When crystals are precipitated by a cooling operation or the like after completion of the reaction, the obtained crystals are separated by filtration, washed with water, alcohol or the like, and then dried under reduced pressure to obtain the compound of this embodiment.

  In the case of a homogeneous solution without crystal precipitation after completion of the reaction, the crystal can be precipitated, for example, by the following method. By adding a carbonate such as sodium carbonate or sodium hydrogen carbonate or a weakly basic aqueous solution containing them to the uniform reaction solution, crystals of bisalkylidene diaminoguanidine or its carbonate precipitate. This is filtered off and the compound of this embodiment can be obtained by the same operation as described above.

  In most cases, the product obtained by the operation of adding the aqueous solution containing the carbonate forms a salt with carbonic acid, but depending on the type of the carbonyl compound used, the salt is not formed unexpectedly. Bisalkylidene diaminoguanidine may be obtained. The carbonyl compound from which bisalkylidene diaminoguanidine that does not form a salt is not particularly limited, and examples thereof include acrolein, isobutyraldehyde, benzylideneacetone, and the carbonyl compound that is obtained as bisalkylidene diaminoguanidine carbonate is not particularly limited. Are methacrolein, crotonaldehyde, and the like.

It can be identified by ¹ H-NMR that the compound represented by formula (1) or formula (2) of this embodiment has a bisalkylidenediaminoguanidine skeleton, and forms a salt with an acid. It can be identified by elemental analysis.

  When the compound represented by the formula (1) or the formula (2) of this embodiment is used as a rubber additive, the low loss property and tensile breaking strength of the vulcanized rubber composition containing an inorganic filler such as silica are obtained. From the viewpoint of improving the melting point, the compound preferably has a melting point of 50 to 300 ° C, more preferably 50 to 200 ° C. When the melting point is 50 to 300 ° C., workability is good because it is solid at ordinary temperature, and when it is 50 to 200 ° C., it tends to melt at the rubber kneading temperature or vulcanization temperature and easily mix with the rubber.

<Modified rubber>
The modified rubber (A) of this embodiment (hereinafter also referred to simply as “modified rubber”) is at least one selected from the group consisting of natural rubber and synthetic rubber (hereinafter referred to as “raw rubber”, simply “rubber”). , Also referred to as “raw material”) is modified with a compound represented by formula (1) or formula (2) (hereinafter also referred to as “rubber modifier” or simply “modifier”). When the modified rubber (A) of the present embodiment is used as a rubber composition containing an inorganic filler such as silica, excellent effects can be exhibited in terms of low loss and breaking strength.

  As the raw rubber of the modified rubber (A) of this embodiment, any of natural rubber, synthetic rubber, and both can be used, but the effect of this embodiment is remarkably obtained especially when natural rubber is used. Can be preferred. Synthetic rubber is a synthetic rubber whose affinity with an inorganic filler is improved by terminal modification with a polar group shown in Patent Document 3, or a polar group-containing single monomer shown in Patent Document 4 This is because natural rubber cannot be used for natural rubber, while it can easily introduce polar groups at the time of polymerization, as in the case of synthetic rubber that has been copolymerized to improve the affinity with inorganic fillers. is there.

  Although it does not specifically limit as natural rubber, Any shape of the sheet rubber and block rubber obtained by coagulating and drying natural rubber latex can be used as a raw material. The seat rubber is not particularly limited, but is classified according to the rating of “International Quality Packaging Standards for Natural Rubber Grades” (commonly called Green Book), and the ribbed smoked sheet (RSS) dried with smoke while being smoked, Examples include a crepe obtained by thoroughly washing an air dry sheet (ADS) coagulated product obtained by drying a sheet with water and drying with hot air. In addition to this, TC rubber (Technically Classified Rubber), SP rubber (Super Processing Rubber), MG Examples include rubber, PP crepe, softener, peptizer-added rubber, and the like. Examples of the block rubber include, but are not limited to, Malaysian SMR (Standard Malaysian Rubber), Indonesian SIR, Thailand TTR, Sri Lanka SCR, Singapore SSR, and the like. These natural rubber raw materials may be used individually by 1 type, and may be used in combination of 2 or more type.

  Moreover, you may use the rubber | gum solidified after oxidizing natural rubber latex, and oxidation of natural rubber latex can be performed by a well-known method. For example, as described in JP-A-8-81505, natural rubber latex dissolved in an organic solvent at a rate of 1.0 to 30% by mass is oxidized in air in the presence of a metal-based oxidation catalyst to oxidize natural rubber latex. It can be performed. Further, as described in JP-A-9-136903, oxidation can be carried out by adding a carbonyl compound to natural rubber latex. When air oxidation is performed as an oxidation method, as described in JP-A-9-136903, air oxidation may be performed in the presence of a radical generator in order to promote air oxidation. The radical generator is not particularly limited, but a peroxide radical generator, a redox radical generator, and an azo radical generator are preferably used.

  The synthetic rubber that can be used as a raw material for the modified rubber (A) is not particularly limited, but 1,4-polybutadiene, 1,2-polybutadiene, 1,4-polyisoprene, 3,4-polyisoprene, styrene butadiene. Examples thereof include diene rubbers having a double bond in the molecule, such as rubber, terminal-modified styrene butadiene rubber, chloroprene rubber, nitrile rubber, ethylene propylene rubber, and ethylene propylene diene rubber.

  In the present embodiment, any of the above-described natural rubber, synthetic rubber, and modified rubber may be used. These may be used alone or in combination of two or more.

（式中、Ｘは、グアニジン部位と塩を形成している酸であり、Ｒ^１及びＲ^２は、それぞれ独立して、炭素数１〜１８のアルキル基、シクロアルキル基、アリール基、アルキルアリール基、及びアルケニル基（これらの基は、いずれも硫黄原子、窒素原子、又は酸素原子を含む置換基を１つ以上有するものを含む）、並びに水素原子からなる群より選択される少なくとも１種である。）

（式中、Ｒ^１及びＲ^２は、それぞれ独立して、炭素数１〜１８のアルキル基、シクロアルキル基、アリール基、アルキルアリール基、及びアルケニル基（これらの基は、いずれも硫黄原子、窒素原子、又は酸素原子を含む置換基を１つ以上有するものを含む）、並びに水素原子からなる群より選択される少なくとも１種である。）The rubber modifier of the present embodiment is a compound represented by the above-described formula (1) or formula (2) (hereinafter also referred to as “bisalkylidene diaminoguanidine salt” or “bisalkylidene diaminoguanidine”).

Wherein X is an acid forming a salt with the guanidine moiety, and R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl A group, and an alkenyl group (all of these groups include those having one or more substituents containing a sulfur atom, a nitrogen atom, or an oxygen atom), and at least one selected from the group consisting of hydrogen atoms is there.)

(In the formula, R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl group, and an alkenyl group (all of these groups are sulfur atoms, Including those having one or more substituents containing a nitrogen atom or an oxygen atom), and at least one selected from the group consisting of hydrogen atoms.)

  When the modified rubber of the present embodiment is used in a rubber composition, the factor that is excellent in low loss property is inferred as follows (however, the factor is not limited to this). In the modified rubber obtained by reacting the modifier with rubber, the hydrazine moiety derived from the modifier is bonded to the rubber. Since the modified rubber has polar groups such as amino groups, the affinity between the polar group of the inorganic filler, particularly in the case of silica, with the silanol group on the silica surface is improved, so that the adhesion between the rubber and the inorganic filler is improved. As a result, when a rubber molded body such as a tire is obtained, the rubber molded body is excellent in low loss. In particular, the guanidine moiety derived from the modifier acts as a polar group of the modified rubber and contributes to improving the adhesion between the rubber and the inorganic filler due to the strong formation of hydrogen bonds with silanol groups on the silica surface. Yes. The formation of this strong hydrogen bond is attributed to the high polarity, basicity, etc. possessed by the guanidine moiety.

  On the other hand, it is surmised that the alkylidene moiety of bisalkylidene diaminoguanidine salt or bisalkylidene diaminoguanidine plays a role in controlling the reactivity of the hydrazine moiety (guanidylamino group) present in the molecule (however, the factor is limited to this) Not) In other words, bisalkylidene diaminoguanidine salt or alkylidene of bisalkylidene diaminoguanidine has a lower reactivity with rubber than that without alkylidene substitution, so it suppresses the increase in rubber viscosity when mixed with rubber and inorganic filler. In addition, workability can be improved.

  Next, a method for producing the modified rubber of this embodiment will be described. The modified rubber of this embodiment can be obtained by mixing the compound represented by the formula (1) or the formula (2) and the rubber using a mixer, an extruder, a kneader or the like. It is preferable to mix with a kneader from the viewpoint of improving dispersibility. As a method of adding the compound represented by formula (1) or formula (2) to a mixer, an extruder, a kneader, etc., a method of adding powder as it is, a method of dissolving in a solvent and adding as a solution, an emulsion solution Any of these methods may be used.

  The reaction conditions for obtaining the modified rubber of the present embodiment are not particularly limited, but it is preferable to mix and modify the rubber and the modifier at a temperature of 20 to 180 ° C, and at a temperature of 50 to 160 ° C. It is more preferable to mix and denature. When the temperature is 20 ° C. to 180 ° C., the rubber and the modifier can be sufficiently mixed, and further, the decomposition of the modifier tends to be suppressed. The rubber kneading time is preferably adjusted to 0.5 to 30 minutes at the reaction temperature, more preferably 2.0 to 10 minutes. If it is 0.5 to 30 minutes, the rubber and the modifier tend to be sufficiently reacted without deteriorating the productivity. The reaction atmosphere is preferably carried out in the presence of oxygen such as air. This is because by kneading in the presence of oxygen, the rubber is partially oxidized and the reactivity with the modifier tends to be improved.

  Further, the modified rubber of the present embodiment can be obtained by mixing the modifier and rubber at once with an extruder, a kneader, etc., or a method using a rubber solidified after oxidizing natural rubber latex, Before adding the modifier, use a technique that applies mechanical force to the raw rubber, called mastication, to loosen the molecular agglomeration (association), cut the molecular chain and adjust the rubber plasticity to a level where it can be easily processed. Is preferable because the reactivity between the modifier and the rubber tends to be improved. In the mastication step, a peptizer (peptizer) may be used.

  The rubber composition can also be obtained by blending various additives appropriately selected as necessary with the modifier, rubber, inorganic filler, and silane coupling agent, and mixing them using a mixer, an extruder, a kneader or the like. Some of the modified rubber is formed inside. This method is preferable in terms of working efficiency than the method of mixing the above modifier and rubber. By performing this operation, the rubber composition of the present embodiment can be obtained.

  The amount of the modifying agent used in producing the modified rubber of the present embodiment is such that the obtained modified rubber has a uniform amount of polar groups introduced into each molecule of the rubber so that the workability is not lowered. From the point that the affinity for fillers such as carbon black is improved and a rubber composition excellent in low loss property is given, it is 0.01 to 10% by mass with respect to the total amount (100% by mass) of the raw rubber. It is preferably 0.1 to 3.0% by mass.

<Rubber composition>
The rubber composition of this embodiment contains a modified rubber (A), a filler containing an inorganic filler (B), and a silane coupling agent (C).

  The rubber composition of this embodiment is obtained by mixing a modified rubber (A), a filler containing an inorganic filler (B), and a silane coupling agent (C). Moreover, the rubber composition of this embodiment is a modified rubber (A) obtained by mixing a modifier, raw rubber, a filler containing an inorganic filler (B), and a silane coupling agent (C). It is good also as a rubber composition containing). Moreover, it is preferable that the temperature at the time of the mixing exists in the range of 20-180 degreeC, and it is more preferable that it exists in the range of 50-160 degreeC. Furthermore, at the time of the mixing, the amount of the modifier used is preferably 0.01 to 10% by mass with respect to the total amount (100% by mass) of the raw rubber, and is preferably 0.1 to 3.0% by mass. More preferably.

  The inorganic filler (B) of this embodiment is an inorganic compound containing at least one selected from silicon, oxides or hydroxides of typical metals or transition metals and hydrates thereof, and carbonates of these metals Point to.

  The inorganic filler (B) is not particularly limited as long as it is an inorganic filler used in the industry. Note that carbon black described later is not included in the inorganic filler (B) here, and does not hit the inorganic filler (B). Inorganic fillers are roughly classified into reinforcing fillers such as silica having active surfaces and surface-treated clay, and non-reinforcing fillers such as calcium carbonate, clay and talc. Specific examples of the inorganic filler (B) include silica, calcium carbonate, magnesium carbonate, aluminum oxide, aluminum hydroxide, aluminum silicate (clay), magnesium silicate (talc), calcium silicate, zinc white, and the like. It is done. Considering the interaction with the modified rubber, it is preferably a reinforcing filler, and more preferably silica. The silica is not particularly limited, and wet silica (hydrous silicic acid), dry silica (anhydrous silicic acid) and the like can be used.

When silica is used, the BET specific surface area is preferably 40 to 350 m ² / g. If the BET specific surface area of silica is in this range, the particle diameter of silica is appropriate, the tensile strength is improved, and the hysteresis loss tends to decrease. The BET specific surface area can be measured according to JIS Z8830: 2013.

  In addition to the inorganic filler (B), carbon black can be added as a filler used in the rubber composition of the present embodiment in order to enhance the reinforcing effect. That is, the filler contains carbon black. Carbon black is a different filler from the inorganic filler (B) and is clearly distinguished from the inorganic filler (B). Although it does not specifically limit as carbon black, The thing of various grades, such as GPF, FEF, SRF, HAF, ISAF, SAF, etc. are mentioned.

  The total content of the inorganic filler (B) and carbon black in the rubber composition of the present embodiment is not particularly limited, but the processability is not deteriorated and a sufficient low loss effect or reinforcing effect is obtained. As content, it is preferable that it exists in the range of 5.0-100 mass parts with respect to 100 mass parts of raw rubber, and it is more preferable that it exists in the range of 20-80 mass parts.

  The silane coupling agent (C) of this embodiment is not particularly limited, but bis (3-triethoxysilylpropyl) tetrasulfide, bis (3-trimethoxysilylpropyl) tetrasulfide, bis (3-methyldimethoxysilyl) Propyl) tetrasulfide, bis (2-triethoxysilylethyl) tetrasulfide, bis (3-triethoxysilylpropyl) disulfide, bis (3-trimethoxysilylpropyl) disulfide, bis (3-triethoxysilylpropyl) trisulfide 3-hexanoylthiopropyltriethoxysilane, 3-octanoylthiopropyltriethoxysilane, 3-decanoylthiopropyltriethoxysilane, 3-lauroylthiopropyltriethoxysilane, 2-hexanoylthioethyl Riethoxysilane, 2-octanoylthioethyltriethoxysilane, 2-decanoylthioethyltriethoxysilane, 2-lauroylthioethyltriethoxysilane, 3-hexanoylthiopropyltrimethoxysilane, 3-octanoylthiopropyltri Methoxysilane, 3-decanoylthiopropyltrimethoxysilane, 3-lauroylthiopropyltrimethoxysilane, 2-hexanoylthioethyltrimethoxysilane, 2-octanoylthioethyltrimethoxysilane, 2-decanoylthioethyltrimethoxy Silane, 2-lauroylthioethyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 3-mercaptopropylmethyldimethoxysilane, 3-aminopro Rutrimethoxysilane, 3-aminopropyltriethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, 3-trimethoxysilylpropyl-N, N-dimethylthiocarbamoyl tetrasulfide, Examples include 3-trimethoxysilylpropylbenzothiazolyl tetrasulfide and 3-trimethoxysilylpropylmethacryloyl monosulfide. The content is preferably 1 to 20 parts by mass with respect to 100 parts by mass of the inorganic filler.

  In addition to the modified rubber, rubber, and inorganic filler, the rubber composition of the present embodiment is not particularly limited as a compounding agent that is usually used in the rubber industry, but is not limited to an anti-aging agent, a softening agent, and a vulcanization accelerator. An agent, a vulcanization acceleration aid, a vulcanizing agent, and the like can be appropriately selected and blended within a range that does not impair the object of the present embodiment. As these compounding agents, commercially available products can be suitably used.

  The type of anti-aging agent is not particularly limited. For example, naphthylamine, p-phenylenediamine, hydroquinone derivatives, bis, tris, polyphenol, diphenylamine, quinoline, monophenol, thiobisphenol, hindered Phenol-based compounds can be used, and p-phenylenediamine-based and diphenylamine-based amine-based antioxidants are preferable from the viewpoint of further anti-aging effects. Although it does not specifically limit as a diphenylamine type | system | group antioxidant, 4,4'-bis ((alpha) -methylbenzyl) diphenylamine, 4,4'-bis ((alpha), alpha-dimethylbenzyl) diphenylamine, p- (p-toluenesulfonyl) Amido) diphenylamine, di (4-octylphenyl) amine and the like. Among these, 4,4′-bis (α-methylbenzyl) diphenylamine is more preferable from the viewpoint of higher anti-aging effect. The p-phenylenediamine anti-aging agent is not particularly limited, but N, N'-diphenyl-p-phenylenediamine, N-isopropyl-N'-phenyl-p-phenylenediamine, N, N'-di 2-naphthyl-p-phenylenediamine, N-cyclohexyl-N′-phenyl-p-phenylenediamine, N-phenyl-N ′-(3-methacryloyloxy-2-hydroxypropyl) -p-phenylenediamine, N, N'-bis (1-methylheptyl) -p-phenylenediamine, N, N'-bis (1,4-dimethylpentyl) -p-phenylenediamine, N, N'-bis (1-ethyl-3-methyl) Pentyl) -p-phenylenediamine, N- (1,3-dimethylbutyl) -N′-phenyl-p-phenylenediamine, and the like. It is, among these, further a high anti-aging effect and cost, N-(1,3-dimethylbutyl)-N'-phenyl -p- phenylenediamine are more preferred. The content of the antioxidant in the rubber composition is preferably 0.1 to 5.0% by mass of the rubber component in the rubber composition.

  The kind of the softener is not particularly limited, and examples thereof include mineral oil-based softeners derived from petroleum and coal tar, vegetable oil-based softeners derived from fatty oils and pine trees, and synthetic resin-based softeners.

  The type of the vulcanization accelerator is not particularly limited, and examples thereof include thiazoles such as mercaptobenzothiazole and 2,2′-dibenzothiazolyl disulfide, N-cyclohexyl-2-benzothiazolylsulfenamide, N, Examples thereof include sulfenamides such as N′-dicyclohexyl-2-benzothiazolylsulfenamide and N′-tert-butyl-2-benzothiazolylsulfenamide, and guanidines such as diphenylguanidine. These vulcanization accelerators may be used alone or in combination of two or more. The content is preferably 0.1 to 5.0 parts by mass with respect to 100 parts by mass of the rubber component. Although it does not specifically limit as a vulcanization | cure acceleration | stimulation adjuvant, For example, a stearic acid and zinc white are mentioned.

  Although it does not specifically limit as a kind of vulcanizing agent, Although what is normally used in this industry can be used suitably, Sulfur, a peroxide, etc. are mentioned, Preferably it is sulfur. The content of the vulcanizing agent is preferably 0.1 to 5.0 parts by mass, more preferably 0.5 to 3.0 parts by mass with respect to 100 parts by mass of the rubber component. When the content of the vulcanizing agent is 0.1 parts by mass or more, sufficient vulcanization tends to be obtained, and when the content of the vulcanizing agent is 5.0 parts by mass or less, so-called It tends to be able to suppress the scorch time from being shortened and the rubber from scoring during kneading.

<Tire>
The tire according to the present embodiment is characterized by using the rubber composition, and the rubber composition is preferably used for a tread of a tire member. A tire using the rubber composition as a tread is excellent in fuel efficiency. The tire of the present embodiment is not particularly limited except that the above rubber composition is used for any of the tire members, and can be manufactured according to a conventional method. Moreover, as gas with which this tire is filled, inert gas, such as nitrogen, argon, helium other than normal or the air which adjusted oxygen partial pressure, can be used.

  The modified rubber of the present embodiment can obtain excellent low loss and breaking strength when a rubber composition containing an inorganic filler such as silica and a tire using the rubber composition are used.

  Hereinafter, the present embodiment will be described in more detail with reference to examples. However, the present embodiment is not limited to the following examples.

５０ｍＬナス型フラスコに、ジアミノグアニジン塩酸塩７８３ｍｇ（東京化成工業株式会社製、６．２ｍｍｏｌ）、水６ｍＬ、１２Ｎ塩酸０．２５ｍＬを加え、室温で１０分間撹拌した後、メチルイソプロピルケトンを１．１０２ｇ（１２．８ｍｍｏｌ）加え、磁気撹拌子を用いて室温で撹拌した。撹拌中に、白色結晶が析出し、２時間撹拌した後、析出した結晶を濾取した。水洗後、５０℃で２２時間真空乾燥して、白色固体を４４５ｍｇ（１．７ｍｍｏｌ）得た。得られた固体を^１Ｈ−ＮＭＲで分析し、ビス（１，２−ジメチルプロピリデン）ジアミノグアニジン塩酸塩であることを確認した（^１Ｈ−ＮＭＲ（ＤＭＳＯ−ｄ６，５００ＭＨｚ，δ；ｐｐｍ）＝２．６−２．５（ｍ；２Ｈ）、１．９（ｓ；６Ｈ）、１．１（ｄｄ；１２Ｈ））。モル収率は２７％であった。また、微量融点測定器ＢＹ−１（（株）矢沢科学製）を用いて融点を測定したところ、１４４−１４５℃であり、炭素・水素・窒素同時定量装置ＣＨＮコーダーＭＴ−６（ヤナコ分析工業（株））を用いて元素分析を行ったところ、計算値Ｃ，５０．４７；Ｈ，９．２４；Ｎ，２６．７５に対し、実測値Ｃ，４９．８４；Ｈ，９．４３；Ｎ，２６．９８であった。Example 1 Synthesis of bis (1,2-dimethylpropylidene) diaminoguanidine hydrochloride (5)

To a 50 mL eggplant-shaped flask were added 783 mg of diaminoguanidine hydrochloride (Tokyo Kasei Kogyo Co., Ltd., 6.2 mmol), 6 mL of water, and 0.25 mL of 12N hydrochloric acid. After stirring at room temperature for 10 minutes, 1.102 g of methyl isopropyl ketone was added. (12.8 mmol) was added and stirred at room temperature using a magnetic stir bar. During the stirring, white crystals were precipitated. After stirring for 2 hours, the precipitated crystals were collected by filtration. After washing with water and vacuum drying at 50 ° C. for 22 hours, 445 mg (1.7 mmol) of a white solid was obtained. The obtained solid was analyzed by ¹ H-NMR and confirmed to be bis (1,2-dimethylpropylidene) diaminoguanidine hydrochloride ( ¹ H-NMR (DMSO-d6, 500 MHz, δ; ppm) = 2.6-2.5 (m; 2H), 1.9 (s; 6H), 1.1 (dd; 12H)). The molar yield was 27%. Moreover, when melting | fusing point was measured using trace amount melting | fusing point measuring device BY-1 (product made from Yazawa Kagaku Co., Ltd.), it was 144-145 degreeC, and carbon, hydrogen, and nitrogen simultaneous determination apparatus CHN coder MT-6 (Yanako analysis industry) Elemental analysis was performed using the calculation value C, 50.47; H, 9.24; N, 26.75, and the measured value C, 49.84; H, 9.43; N, 26.98.

５０ｍＬナス型フラスコに、ジアミノグアニジン塩酸塩７５９ｍｇ（６．０ｍｍｏｌ）、水６ｍＬ、１２Ｎ塩酸０．２５ｍＬを加え、室温で１０分間撹拌した後、２−ヘキサノンを１．２１ｇ（１２．１ｍｍｏｌ）加え、磁気撹拌子を用いて室温で撹拌した。撹拌中に、白色結晶が析出し、２時間撹拌した後、析出した結晶を濾取した。水洗後、５０℃で１６時間真空乾燥して、白色固体を１．１８ｇ（４．１ｍｍｏｌ）得た。得られた固体を^１Ｈ−ＮＭＲで分析し、ビス（１−メチルペンチリデン）ジアミノグアニジン塩酸塩であることを確認した（^１Ｈ−ＮＭＲ（ＤＭＳＯ−ｄ６，５００ＭＨｚ，δ；ｐｐｍ）＝０．９（ｍ；６Ｈ）、１．２−１．３（ｍ；４Ｈ）、１．４−１．５（ｍ；４Ｈ）、２．０（ｓ；６Ｈ）、２．３（ｔ；４Ｈ）、８．０−８．２（ｂｒ））。モル収率は６８％であった。また、微量融点測定器ＢＹ−１（（株）矢沢科学製）を用いて融点を測定したところ、１００−１０１℃であり、炭素・水素・窒素同時定量装置ＣＨＮコーダーＭＴ−６（ヤナコ分析工業（株））を用いて元素分析を行ったところ、計算値Ｃ，５３．８７；Ｈ，９．７４；Ｎ，２４．１６に対し、実測値Ｃ，５３．４６；Ｈ，１０．０３；Ｎ，２４．３１であった。Example 2 Synthesis of bis (1-methylpentylidene) diaminoguanidine hydrochloride (6)

To a 50 mL eggplant-shaped flask, 759 mg (6.0 mmol) of diaminoguanidine hydrochloride, 6 mL of water, and 0.25 mL of 12N hydrochloric acid were added, stirred for 10 minutes at room temperature, and then 1.21 g (12.1 mmol) of 2-hexanone was added. Stir at room temperature using a magnetic stir bar. During the stirring, white crystals were precipitated. After stirring for 2 hours, the precipitated crystals were collected by filtration. After washing with water and vacuum drying at 50 ° C. for 16 hours, 1.18 g (4.1 mmol) of a white solid was obtained. The obtained solid was analyzed by ¹ H-NMR and confirmed to be bis (1-methylpentylidene) diaminoguanidine hydrochloride ( ¹ H-NMR (DMSO-d6, 500 MHz, δ; ppm) = 0. 9 (m; 6H), 1.2-1.3 (m; 4H), 1.4-1.5 (m; 4H), 2.0 (s; 6H), 2.3 (t; 4H) , 8.0-8.2 (br)). The molar yield was 68%. Moreover, when melting | fusing point was measured using trace amount melting | fusing point measuring device BY-1 (made by Yazawa Kagaku Co., Ltd.), it is 100-101 degreeC, and it is carbon, hydrogen, and nitrogen simultaneous determination apparatus CHN coder MT-6 (Yanako analysis industry). The elemental analysis was carried out using the calculated value C, 53.87; H, 9.74; N, 24.16, and the measured value C, 53.46; H, 10.03; N, 24.31.

５０ｍＬナス型フラスコに、ジアミノグアニジン塩酸塩７４１ｍｇ（５．９ｍｍｏｌ）、水６ｍＬ、１２Ｎ塩酸０．２５ｍＬを加え、室温で１０分間撹拌した後、２−ヘプタノンを１．３７ｇ（１２．０ｍｍｏｌ）加え、磁気撹拌子を用いて室温で撹拌した。撹拌中に、白色結晶が析出し、２時間撹拌した後、析出した結晶を濾取した。水及びヘキサンで洗浄後、５０℃で１５時間真空乾燥して、白色固体を１．５１ｇ（４．８ｍｍｏｌ）得た。得られた固体を^１Ｈ−ＮＭＲで分析し、ビス（１−メチルヘキシリデン）ジアミノグアニジン塩酸塩であることを確認した（^１Ｈ−ＮＭＲ（ＤＭＳＯ−ｄ６，５００ＭＨｚ，δ；ｐｐｍ）＝０．９（ｔ；６Ｈ）、１．２−１．３（ｍ；８Ｈ）、１．５−１．６（ｍ；４Ｈ）、１．９（ｓ；６Ｈ）、２．３（ｔ；４Ｈ）、８．１（ｂｒ））。モル収率は８１％であった。また、微量融点測定器ＢＹ−１（（株）矢沢科学製）を用いて融点を測定したところ、１００−１０２℃であり、炭素・水素・窒素同時定量装置ＣＨＮコーダーＭＴ−６（ヤナコ分析工業（株））を用いて元素分析を行ったところ、計算値Ｃ，５６．６７；Ｈ，１０．１５；Ｎ，２２．０３に対し、実測値Ｃ，５６．７４；Ｈ，１０．６０；Ｎ，２２．１０であった。Example 3 Synthesis of bis (1-methylhexylidene) diaminoguanidine hydrochloride (7)

To a 50 mL eggplant-shaped flask, 741 mg (5.9 mmol) of diaminoguanidine hydrochloride, 6 mL of water, and 0.25 mL of 12N hydrochloric acid were added and stirred at room temperature for 10 minutes, and then 1.37 g (12.0 mmol) of 2-heptanone was added, Stir at room temperature using a magnetic stir bar. During the stirring, white crystals were precipitated. After stirring for 2 hours, the precipitated crystals were collected by filtration. After washing with water and hexane, it was vacuum dried at 50 ° C. for 15 hours to obtain 1.51 g (4.8 mmol) of a white solid. The obtained solid was analyzed by ¹ H-NMR and confirmed to be bis (1-methylhexylidene) diaminoguanidine hydrochloride ( ¹ H-NMR (DMSO-d6, 500 MHz, δ; ppm) = 0 .9 (t; 6H), 1.2-1.3 (m; 8H), 1.5-1.6 (m; 4H), 1.9 (s; 6H), 2.3 (t; 4H) ), 8.1 (br)). The molar yield was 81%. Moreover, when melting | fusing point was measured using trace amount melting | fusing point measuring device BY-1 (made by Yazawa Kagaku Co., Ltd.), it is 100-102 degreeC, and it is carbon, hydrogen, and nitrogen simultaneous determination apparatus CHN coder MT-6 (Yanako analysis industry). (Inc.) was used to conduct an elemental analysis. As a result, the calculated value C, 56.67; H, 10.15; N, 22.03, and the measured value C, 56.74; H, 10.60; N, 22.10.

５０ｍＬナス型フラスコに、ジアミノグアニジン塩酸塩１．５０ｇ（１１．９ｍｍｏｌ）、水１２ｍＬ、１２Ｎ塩酸０．１ｍＬを加え、室温で１０分間撹拌した後、メタクロレインを１．８０ｇ（２５．７ｍｍｏｌ）加え、磁気撹拌子を用いて室温で撹拌した。撹拌中に結晶が析出し、１時間撹拌した後、反応液に飽和炭酸水素ナトリウム水溶液２０ｍＬを加えた。析出した結晶を濾取、水洗後、５０℃で２０時間真空乾燥して、白色固体を９２２ｍｇ（３．６ｍｍｏｌ）得た。得られた固体を^１Ｈ−ＮＭＲで分析し、ビス（２−メチルアリリデン）ジアミノグアニジン炭酸塩であることを確認した（^１Ｈ−ＮＭＲ（ＤＭＳＯ−ｄ６，５００ＭＨｚ，δ；ｐｐｍ）＝２．０（ｓ；６Ｈ）、５．５（ｓ；２Ｈ）、５．６（ｓ；２Ｈ）、８．１（ｓ；２Ｈ）、８．２（ｂｒ））。モル収率は３０％であった。また、微量融点測定器ＢＹ−１（（株）矢沢科学製）を用いて融点を測定したところ、融点は観測されなかった。炭素・水素・窒素同時定量装置ＣＨＮコーダーＭＴ−６（ヤナコ分析工業（株））を用いて元素分析を行ったところ、計算値Ｃ，４７．０５；Ｈ，６．７１；Ｎ，２７．４３に対し、実測値Ｃ，４５．６０；Ｈ，７．２２；Ｎ，２９．５４であった。(Example 4) Synthesis of bis (2-methylarylidene) diaminoguanidine carbonate (8)

To a 50 mL eggplant-shaped flask was added 1.50 g (11.9 mmol) of diaminoguanidine hydrochloride, 12 mL of water, and 0.1 mL of 12N hydrochloric acid, and the mixture was stirred at room temperature for 10 minutes, and then 1.80 g (25.7 mmol) of methacrolein was added. The mixture was stirred at room temperature using a magnetic stir bar. Crystals precipitated during stirring, and after stirring for 1 hour, 20 mL of a saturated aqueous sodium hydrogen carbonate solution was added to the reaction solution. The precipitated crystals were collected by filtration, washed with water, and dried in vacuo at 50 ° C. for 20 hours to obtain 922 mg (3.6 mmol) of a white solid. The obtained solid was analyzed by ¹ H-NMR and confirmed to be bis (2-methylallylidene) diaminoguanidine carbonate ( ¹ H-NMR (DMSO-d6, 500 MHz, δ; ppm) = 2. 0 (s; 6H), 5.5 (s; 2H), 5.6 (s; 2H), 8.1 (s; 2H), 8.2 (br)). The molar yield was 30%. Moreover, when melting | fusing point was measured using trace amount melting | fusing point measuring device BY-1 (made by Yazawa Kagaku Co., Ltd.), melting | fusing point was not observed. When elemental analysis was performed using a carbon / hydrogen / nitrogen simultaneous determination apparatus CHN Coder MT-6 (Yanako Analytical Co., Ltd.), the calculated values were C, 47.05; H, 6.71; N, 27.43. On the other hand, it was measured value C, 45.60; H, 7.22; N, 29.54.

５０ｍＬナス型フラスコに、ジアミノグアニジン塩酸塩１．５１ｇ（１２．０ｍｍｏｌ）、水１２ｍＬ、１２Ｎ塩酸０．１ｍＬを加え、室温で１０分間撹拌した後、クロトンアルデヒドを１．７５ｇ（２５．０ｍｍｏｌ）加え、磁気撹拌子を用いて室温で撹拌した。撹拌中に結晶が析出し、１時間撹拌した後、反応液に水２０ｍＬを加えた。析出した結晶を濾取、水洗後、５０℃で２０時間真空乾燥して、白色固体を９１９ｍｇ（３．６ｍｍｏｌ）得た。得られた固体を^１Ｈ−ＮＭＲで分析し、ビス（３−メチルアリリデン）ジアミノグアニジン炭酸塩であることを確認した（^１Ｈ−ＮＭＲ（ＤＭＳＯ−ｄ６，５００ＭＨｚ，δ；ｐｐｍ）＝１．９（ｄ；６Ｈ）、６．２（ｍ；２Ｈ）、６．３（ｍ；２Ｈ）、８．０（ｄ；２Ｈ）、８．１（ｓ；２Ｈ）、１１．８−１２．０（ｂｒ））。モル収率は３０％であった。また、微量融点測定器ＢＹ−１（（株）矢沢科学製）を用いて融点を測定したところ、１６８−１６９℃であり、炭素・水素・窒素同時定量装置ＣＨＮコーダーＭＴ−６（ヤナコ分析工業（株））を用いて元素分析を行ったところ、計算値Ｃ，４７．０５；Ｈ，６．７１；Ｎ，２７．４３に対し、実測値Ｃ，４６．４８；Ｈ，７．１０；Ｎ，３０．０９であった。Example 5 Synthesis of bis (3-methylarylidene) diaminoguanidine carbonate (9)

To a 50 mL eggplant-shaped flask, 1.51 g (12.0 mmol) of diaminoguanidine hydrochloride, 12 mL of water, and 0.1 mL of 12N hydrochloric acid were added and stirred at room temperature for 10 minutes, and then 1.75 g (25.0 mmol) of crotonaldehyde was added. The mixture was stirred at room temperature using a magnetic stir bar. Crystals precipitated during stirring, and after stirring for 1 hour, 20 mL of water was added to the reaction solution. The precipitated crystals were collected by filtration, washed with water, and then vacuum-dried at 50 ° C. for 20 hours to obtain 919 mg (3.6 mmol) of a white solid. The obtained solid was analyzed by ¹ H-NMR and confirmed to be bis (3-methylallylidene) diaminoguanidine carbonate ( ¹ H-NMR (DMSO-d6, 500 MHz, δ; ppm) = 1. 9 (d; 6H), 6.2 (m; 2H), 6.3 (m; 2H), 8.0 (d; 2H), 8.1 (s; 2H), 11.8-12.0 (Br)). The molar yield was 30%. Moreover, when melting | fusing point was measured using trace amount melting | fusing point measuring device BY-1 (product made from Yazawa Kagaku Co., Ltd.), it was 168-169 degreeC, and carbon, hydrogen, and nitrogen simultaneous determination apparatus CHN coder MT-6 (Yanako analysis industry) Elemental analysis was performed using the calculated value C, 47.05; H, 6.71; N, 27.43, and the measured value C, 46.48; H, 7.10; N, 30.09.

５０ｍＬナス型フラスコに、ジアミノグアニジン塩酸塩７５２ｍｇ（６．０ｍｍｏｌ）、メタノール６ｍＬ、１２Ｎ塩酸０．２５ｍＬを加え、室温で１０分間撹拌した後、ベンジリデンアセトンを１．６３３ｇ（１１．２ｍｍｏｌ）加え、磁気撹拌子を用いて室温で撹拌した。撹拌開始後、直ちに黄色結晶が析出し、２時間撹拌した後、析出した結晶を濾取、水洗後、５０℃で１７時間真空乾燥して、黄色固体を１．９４ｇ（５．１ｍｍｏｌ）得た。得られた固体を^１Ｈ−ＮＭＲで分析し、ビス（１−メチル−３−フェニルアリリデン）ジアミノグアニジン塩酸塩であることを確認した（^１Ｈ−ＮＭＲ（ＤＭＳＯ−ｄ６，５００ＭＨｚ，δ；ｐｐｍ）＝２．２（ｓ；６Ｈ）、７．０（ｄ；２Ｈ）、７．３（ｄ；２Ｈ）、７．３（ｔ；２Ｈ）、７．４（ｔ；４Ｈ）、７．６（ｄ；４Ｈ）、８．５−８．６（ｂｒ）、１１．６−１１．７（ｂｒ））。モル収率は８５％であった。また、微量融点測定器ＢＹ−１（（株）矢沢科学製）を用いて融点を測定したところ、２６３−２６５℃であり、炭素・水素・窒素同時定量装置ＣＨＮコーダーＭＴ−６（ヤナコ分析工業（株））を用いて元素分析を行ったところ、計算値Ｃ，６４．８５；Ｈ，６．１８；Ｎ，１７．１９に対し、実測値Ｃ，６６．０４；Ｈ，６．３３；Ｎ，１８．３４であった。Example 6 Synthesis of bis (1-methyl-3-phenylallylidene) diaminoguanidine hydrochloride (10)

To a 50 mL eggplant-shaped flask was added 752 mg (6.0 mmol) of diaminoguanidine hydrochloride, 6 mL of methanol, and 0.25 mL of 12N hydrochloric acid, and the mixture was stirred at room temperature for 10 minutes, and then 1.633 g (11.2 mmol) of benzylideneacetone was added. Stir at room temperature using a stir bar. After the start of stirring, yellow crystals were immediately precipitated, and after stirring for 2 hours, the precipitated crystals were collected by filtration, washed with water, and vacuum dried at 50 ° C. for 17 hours to obtain 1.94 g (5.1 mmol) of a yellow solid. . The obtained solid was analyzed by ¹ H-NMR and confirmed to be bis (1-methyl-3-phenylallylidene) diaminoguanidine hydrochloride ( ¹ H-NMR (DMSO-d6, 500 MHz, δ; ppm ) = 2.2 (s; 6H), 7.0 (d; 2H), 7.3 (d; 2H), 7.3 (t; 2H), 7.4 (t; 4H), 7.6 (D; 4H), 8.5-8.6 (br), 11.6-11.7 (br)). The molar yield was 85%. Moreover, when melting | fusing point was measured using trace melting | fusing point measuring device BY-1 (made by Yazawa Kagaku Co., Ltd.), it was 263-265 degreeC, and it was a carbon, hydrogen, and nitrogen simultaneous determination apparatus CHN coder MT-6 (Yanako analysis industry). Elemental analysis was performed using the calculated value C, 64.85; H, 6.18; N, 17.19, and the measured value C, 66.04; H, 6.33; N, 18.34.

５０ｍＬナス型フラスコに、ジアミノグアニジン塩酸塩７４１ｍｇ（５．９ｍｍｏｌ）、メタノール６ｍＬ、１２Ｎ塩酸０．２５ｍＬを加え、室温で１０分間撹拌した後、イソブチルアルデヒドを８６１ｍｇ（１１．９ｍｍｏｌ）加え、磁気撹拌子を用いて室温で撹拌した。２時間撹拌した後、反応液に飽和炭酸水素ナトリウム水溶液２０ｍＬを加えた。析出した結晶を濾取、水洗後、５０℃で１５時間真空乾燥して、黄色固体を３２１ｍｇ（１．６ｍｍｏｌ）得た。得られた固体を^１Ｈ−ＮＭＲで分析し、ビス（２−メチルプロピリデン）ジアミノグアニジンであることを確認した^１Ｈ−ＮＭＲ（ＤＭＳＯ−ｄ６，５００ＭＨｚ，δ；ｐｐｍ）＝１．０（ｄｄ；１２Ｈ）、２．４−２．５（ｍ；２Ｈ）、５．８（ｓ；２Ｈ）、７．２（ｄｄ；２Ｈ）、９．８（ｂｒ））。モル収率は２８％であった。また、微量融点測定器ＢＹ−１（（株）矢沢科学製）を用いて融点を測定したところ、６５−６７℃であり、炭素・水素・窒素同時定量装置ＣＨＮコーダーＭＴ−６（ヤナコ分析工業（株））を用いて元素分析を行ったところ、計算値Ｃ，５４．７９；Ｈ，９．７１；Ｎ，３５．５０に対し、実測値Ｃ，５４．５６；Ｈ，１０．０２；Ｎ，３５．０７であった。Example 7 Synthesis of bis (2-methylpropylidene) diaminoguanidine (11)

To a 50 mL eggplant-shaped flask, 741 mg (5.9 mmol) of diaminoguanidine hydrochloride, 6 mL of methanol, and 0.25 mL of 12N hydrochloric acid were added and stirred at room temperature for 10 minutes. Then, 861 mg (11.9 mmol) of isobutyraldehyde was added, And stirred at room temperature. After stirring for 2 hours, 20 mL of a saturated aqueous sodium hydrogen carbonate solution was added to the reaction solution. The precipitated crystals were collected by filtration, washed with water, and then vacuum dried at 50 ° C. for 15 hours to obtain 321 mg (1.6 mmol) of a yellow solid. The obtained solid was analyzed by ¹ H-NMR and confirmed to be bis (2-methylpropylidene) diaminoguanidine ¹ H-NMR (DMSO-d6, 500 MHz, δ; ppm) = 1.0 (dd 12H), 2.4-2.5 (m; 2H), 5.8 (s; 2H), 7.2 (dd; 2H), 9.8 (br)). The molar yield was 28%. Moreover, when melting | fusing point was measured using trace amount melting | fusing point measuring device BY-1 (made by Yazawa Kagaku Co., Ltd.), it was 65-67 degreeC, and carbon, hydrogen, and nitrogen simultaneous determination apparatus CHN coder MT-6 (Yanako analysis industry) The elemental analysis was carried out using the calculated value C, 54.79; H, 9.71; N, 35.50, the measured value C, 54.56; H, 10.02. N, 35.07.

５０ｍＬナス型フラスコに、ジアミノグアニジン塩酸塩７５４ｍｇ（６．０ｍｍｏｌ）、水６ｍＬ、１２Ｎ塩酸０．０５ｍＬを加え、室温で１０分間撹拌した後、アクロレインを１．０１ｇ（１８．０ｍｍｏｌ）加え、磁気撹拌子を用いて室温で撹拌した。撹拌開始後、１時間後に結晶が析出し、４時間撹拌した後、反応液に飽和炭酸水素ナトリウム水溶液２０ｍＬを加えた。析出した結晶を濾取、水洗後、５０℃で２０時間真空乾燥して、白色固体を３３１ｍｇ（２．０ｍｍｏｌ）得た。得られた固体を^１Ｈ−ＮＭＲで分析し、ビスアリリデンジアミノグアニジンであることを確認した（^１Ｈ−ＮＭＲ（ＤＭＳＯ−ｄ６，５００ＭＨｚ，δ；ｐｐｍ）＝５．４（ｄ；２Ｈ）、５．５（ｄ；２Ｈ）、６．５（ｄｄｄ；２Ｈ）、６．０−６．３（ｂｒ）、７．７（ｄ；２Ｈ））。モル収率は３３％であった。また、微量融点測定器ＢＹ−１（（株）矢沢科学製）を用いて融点を測定したところ、１４９−１５２℃であり、炭素・水素・窒素同時定量装置ＣＨＮコーダーＭＴ−６（ヤナコ分析工業（株））を用いて元素分析を行ったところ、計算値Ｃ，５０．８９；Ｈ，６．７１；Ｎ，４２．３９に対し、実測値Ｃ，５０．０３；Ｈ，６．６８；Ｎ，４１．２７であった。重合開始温度を示差走査熱量測定装置（セイコーインスツル（株）製ＤＳＣ６２２０、１０℃／ｍｉｎ）で重合による発熱ピークが立ち上がる時点の温度として求めたところ、１５０℃であった。Example 8 Synthesis of bisarylidenediaminoguanidine (12)

To a 50 mL eggplant-shaped flask, 754 mg (6.0 mmol) of diaminoguanidine hydrochloride, 6 mL of water, and 0.05 mL of 12N hydrochloric acid were added. After stirring at room temperature for 10 minutes, 1.01 g (18.0 mmol) of acrolein was added and magnetic stirring was performed. It stirred at room temperature using the child. Crystals precipitated after 1 hour from the start of stirring, and after stirring for 4 hours, 20 mL of a saturated aqueous solution of sodium bicarbonate was added to the reaction solution. The precipitated crystals were collected by filtration, washed with water, and then vacuum dried at 50 ° C. for 20 hours to obtain 331 mg (2.0 mmol) of a white solid. The obtained solid was analyzed by ¹ H-NMR and confirmed to be bisarylidenediaminoguanidine ( ¹ H-NMR (DMSO-d6, 500 MHz, δ; ppm) = 5.4 (d; 2H), 5.5 (d; 2H), 6.5 (ddd; 2H), 6.0-6.3 (br), 7.7 (d; 2H)). The molar yield was 33%. Moreover, when melting | fusing point was measured using trace amount melting | fusing point measuring device BY-1 (made by Yazawa Kagaku Co., Ltd.), it was 149-152 degreeC, and carbon, hydrogen, and nitrogen simultaneous determination apparatus CHN coder MT-6 (Yanako analysis industry) The elemental analysis was carried out using the calculated value C, 50.89; H, 6.71; N, 42.39, the measured value C, 50.03; H, 6.68; N, 41.27. The polymerization initiation temperature was determined to be 150 ° C. when it was determined as the temperature at which the exothermic peak due to polymerization rose with a differential scanning calorimeter (DSC 6220 manufactured by Seiko Instruments Inc., 10 ° C./min).

５０ｍＬナス型フラスコに、ジアミノグアニジン塩酸塩７５４ｍｇ（６．０ｍｍｏｌ）、メタノール６ｍＬ、１２Ｎ塩酸０．２５ｍＬを加え、室温で１０分間撹拌した後、ベンジリデンアセトンを１．７９ｇ（１２．２ｍｍｏｌ）加え、磁気撹拌子を用いて室温で撹拌した。撹拌開始後、直ちに黄色結晶が析出し、２時間撹拌した後、反応液に飽和炭酸水素ナトリウム水溶液２０ｍＬを加えた。析出した結晶を濾取、水洗後、５０℃で１５時間真空乾燥して、黄色固体を１．７３ｇ（５．０ｍｍｏｌ）得た。得られた固体を^１Ｈ−ＮＭＲで分析し、ビス（１−メチル−３−フェニルアリリデン）ジアミノグアニジンであることを確認した（^１Ｈ−ＮＭＲ（ＡＣＥＴＯＮＥ−ｄ６，５００ＭＨｚ，δ；ｐｐｍ）＝２．２（ｓ；６Ｈ）、６．９−７．１（ｍ；４Ｈ）、７．３（ｔ；２Ｈ）、７．４（ｔ；４Ｈ）、７．６（ｄ；４Ｈ）、））。モル収率は８３％であった。また、微量融点測定器ＢＹ−１（（株）矢沢科学製）を用いて融点を測定したところ、８１−８３℃、１６０−１６３℃であり、炭素・水素・窒素同時定量装置ＣＨＮコーダーＭＴ−６（ヤナコ分析工業（株））を用いて元素分析を行ったところ、計算値Ｃ，７３．０２；Ｈ，６．７１；Ｎ，２０．２７に対し、実測値Ｃ，７１．５７；Ｈ，８．９８；Ｎ，１９．５４であった。Example 9 Synthesis of bis (1-methyl-3-phenylallylidene) diaminoguanidine (13)

To a 50 mL eggplant-shaped flask, 754 mg (6.0 mmol) of diaminoguanidine hydrochloride, 6 mL of methanol, and 0.25 mL of 12N hydrochloric acid were added. After stirring at room temperature for 10 minutes, 1.79 g (12.2 mmol) of benzylideneacetone was added, Stir at room temperature using a stir bar. After the stirring was started, yellow crystals were immediately precipitated, and after stirring for 2 hours, 20 mL of a saturated aqueous sodium hydrogen carbonate solution was added to the reaction solution. The precipitated crystals were collected by filtration, washed with water, and vacuum dried at 50 ° C. for 15 hours to obtain 1.73 g (5.0 mmol) of a yellow solid. The obtained solid was analyzed by ¹ H-NMR and confirmed to be bis (1-methyl-3-phenylarylidene) diaminoguanidine ( ¹ H-NMR (ACENETE-d6, 500 MHz, δ; ppm) = 2.2 (s; 6H), 6.9-7.1 (m; 4H), 7.3 (t; 2H), 7.4 (t; 4H), 7.6 (d; 4H),) ). The molar yield was 83%. Moreover, when melting | fusing point was measured using trace amount melting | fusing point measuring device BY-1 (made by Yazawa Kagaku Co., Ltd.), they are 81-83 degreeC and 160-163 degreeC, and carbon, hydrogen, and nitrogen simultaneous determination apparatus CHN coder MT- 6 (Yanako Analytical Industrial Co., Ltd.) was used for elemental analysis, and calculated values C, 73.02; H, 6.71; N, 20.27, and measured values C, 71.57; H , 8.98; N, 19.54.

１００ｍＬナス型フラスコに、ジアミノグアニジン塩酸塩３．０１９ｇ（２４ｍｍｏｌ）、水１２ｍＬ、１２Ｎ塩酸０．１ｍＬを加え、室温で１０分間撹拌した後、メチルエチルケトンを４．０８７ｇ（５７ｍｍｏｌ）加え、磁気撹拌子を用いて室温で撹拌した。撹拌を開始して間もなく白色結晶が析出し、０．５時間撹拌した後、反応液をろ過、水洗後、５０℃で１６時間真空乾燥して、白色結晶を４．４１０ｇ（１９ｍｍｏｌ）得た。得られた固体を^１Ｈ−ＮＭＲで分析し、ビス（１−メチルプロピリデン）ジアミノグアニジン塩酸塩であることを確認した（^１Ｈ−ＮＭＲ（ＤＭＳＯ−ｄ６，５００ＭＨｚ，δ；ｐｐｍ）＝１．１（ｔ；６Ｈ）、２．０（ｓ；６Ｈ）、２．３（ｑ；４Ｈ））。モル収率は７９％であった。また、微量融点測定器ＢＹ−１（（株）矢沢科学製）を用いて融点を測定したところ、１３３−１３４℃であり、炭素・水素・窒素同時定量装置ＣＨＮコーダーＭＴ−６（ヤナコ分析工業（株））を用いて元素分析を行ったところ、計算値Ｃ，４６．２５；Ｈ，８．６２；Ｎ，２９．９６に対し、実測値Ｃ，４６．０２；Ｈ，９．０５；Ｎ，２９．９８であった。Example 10 Synthesis of bis (1-methylpropylidene) diaminoguanidine hydrochloride (14)

To a 100 mL eggplant-shaped flask, 3.019 g (24 mmol) of diaminoguanidine hydrochloride, 12 mL of water, and 0.1 mL of 12N hydrochloric acid were added and stirred at room temperature for 10 minutes, and then 4.087 g (57 mmol) of methyl ethyl ketone was added, and a magnetic stirrer was added. And stirred at room temperature. Soon after the start of stirring, white crystals were precipitated, and after stirring for 0.5 hours, the reaction solution was filtered, washed with water, and then vacuum-dried at 50 ° C. for 16 hours to obtain 4.410 g (19 mmol) of white crystals. The obtained solid was analyzed by ¹ H-NMR and confirmed to be bis (1-methylpropylidene) diaminoguanidine hydrochloride ( ¹ H-NMR (DMSO-d6, 500 MHz, δ; ppm) = 1. 1 (t; 6H), 2.0 (s; 6H), 2.3 (q; 4H)). The molar yield was 79%. Moreover, when melting | fusing point was measured using trace melting | fusing point measuring device BY-1 (made by Yazawa Kagaku Co., Ltd.), it was 133-134 degreeC, and carbon, hydrogen, and nitrogen simultaneous determination apparatus CHN coder MT-6 (Yanako analysis industry) Elemental analysis was performed using the calculated value C, 46.25; H, 8.62; N, 29.96, and the measured value C, 46.02; H, 9.05; N, 29.98.

(Example 11)
41.4 g of natural rubber coagulum (RSS # 1, manufactured by Kato Sansho Co., Ltd.) is put into a lab plast mill (manufactured by Toyo Seiki Seisakusho Co., Ltd.) heated to 30 ° C. in a mixer, and rotated at 60 rpm. The kneading was carried out for 1 minute with the lid closed, and for 4 minutes with the lid opened. When the temperature of the rubber rose to 80 ° C. due to shearing heat generation, 0.414 g (1.77 mmol) of bis (1-methylpropylidene) diaminoguanidine hydrochloride obtained in Example 10 was added and kneaded for 3 minutes. Thus, modified rubber 1 was obtained. At this time, the temperature of the rubber had reached 85 ° C.

  The modified rubber 1 (9.0 g) was heated to reflux in 200 g of a 2: 1 mixed solvent of acetone and methanol for 2 hours to extract unreacted 1,3-diaminoguanidine hydrochloride. After the solvent was distilled off under reduced pressure, the residue was quantitatively analyzed by liquid chromatography. As a result, 0.0048 g (0.021 mmol) of bis (1-methylpropylidene) diaminoguanidine hydrochloride and bis (1-methylethylidene) diaminoguanidine were obtained. 0.0047 g (0.023 mmol, 0.0053 g in terms of bis (1-methylpropylidene) diaminoguanidine hydrochloride) was contained. That is, the total amount of unreacted bis (1-methylpropylidene) aminoguanidine hydrochloride was 0.0101 g (0.043 mmol). The bis (1-methylpropylidene) diaminoguanidine hydrochloride contained in the modified rubber 1 (9.0 g) before elution is 0.0891 g (0.381 mmol), and 89 mol% of the added diaminoguanidine hydrochloride is natural. Reacted with rubber.

  Therefore, it was confirmed that the added amount of bis (1-methylpropylidene) diaminoguanidine in the modified rubber 1 was 0.1% by mass with respect to the solid rubber component in the natural rubber raw material.

(Reference Example 1)
41.4 g of natural rubber coagulated body (RSS # 1) is put into a lab plast mill heated to 30 ° C. in the mixer, and the lid is closed at 60 rpm for 1 minute, and the lid is opened for 4 minutes. Kneaded. After the temperature of the rubber reached 80 ° C. due to shearing heat generation, kneading was further performed for 3 minutes to obtain an unmodified rubber 1. At this time, the temperature of the rubber had reached 85 ° C.

(Example 12, Comparative Example 1)
According to the composition of Table 1, first, the modified rubber 1 or unmodified rubber 1, silica, silane coupling agent, zinc white, and stearic acid were kneaded at 140 ° C. for 5 minutes in the above Laboplast mill, and then once heated to 55 ° C. After cooling, sulfur and a vulcanization accelerator were added thereto and kneaded at 90 ° C. for 3 minutes to prepare a rubber composition. Subsequently, a vulcanized rubber composition was obtained by vulcanization at 145 ° C. and 10 MPa for 38 to 44 minutes using a press machine (manufactured by Kitagawa Seiki Co., Ltd.). It shows about the component used below.
Silica: Trade name “Nip seal AQ” (BET specific surface area = 207 m ² / g, manufactured by Tosoh Silica Co., Ltd.)
Silane coupling agent: bis (3-triethoxysilylpropyl) tetrasulfide (manufactured by Evonik Japan Co., Ltd.)
Zinc flower (Wako Pure Chemical Industries, Ltd.)
Stearic acid (Wako Pure Chemical Industries, Ltd.)
Sulfur (Hosoi Chemical Co., Ltd., 250 μm)
Vulcanization accelerator (CBS): N-cyclohexyl-2-benzothiazolylsulfenamide (Wako Pure Chemical Industries, Ltd.)
Vulcanization accelerator (DPG): Diphenylguanidine (manufactured by Wako Pure Chemical Industries, Ltd.)

(Example 13, Comparative Example 2)
According to the composition of Table 2, after natural rubber coagulated body (RSS # 1), silica, silane coupling agent, zinc white, stearic acid, and modifier 1 are kneaded at 140 ° C. for 5 minutes in the above lab plast mill. Once cooled to 55 ° C., sulfur and a vulcanization accelerator were added thereto and kneaded. After reaching 90 ° C., the mixture was further kneaded for 3 minutes to prepare a rubber composition. Subsequently, a vulcanized rubber composition was obtained by vulcanization at 145 ° C. and 10 MPa for 35 to 42 minutes using a press machine (Kitakawa Seiki Co., Ltd.). The components used are shown below (the same applies to those used in Table 1).
Denaturant 1: 1,3-diaminoguanidine hydrochloride (manufactured by Tokyo Chemical Industry Co., Ltd.)

With respect to the vulcanized rubber composition, the exothermic property and tensile breaking strength were measured and evaluated by the following methods. The results are shown in Tables 1 and 2.
(1) Exothermicity The loss tangent (tan δ) of the vulcanized rubber composition was measured using a dynamic viscoelasticity measuring device (DMS6100 manufactured by Seiko Instruments Inc.) at a temperature of 50 ° C., a strain of 0.5%, and a frequency of 10 Hz. ) Was measured, and the values of Comparative Example 1 in Table 1 and Comparative Example 2 in Table 2 were taken as 100, and each index was displayed. The smaller the index value, the lower the tan δ, indicating that the rubber composition is less exothermic.
(2) Tensile strength at break The above vulcanized rubber composition was subjected to a tensile test according to JIS K6251: 2010, and the tensile strength at break was measured. Values of Comparative Example 1 in Table 1 and Comparative Example 2 in Table 2 The index was expressed as 100. A larger index value indicates a higher tensile breaking strength.

表１中、配合処方の各成分は質量部を示す。

In Table 1, each component of the compounding prescription indicates part by mass.

  From Table 1, the rubber compositions of the examples are excellent in low heat buildup and have a high tensile breaking strength as compared with a rubber composition mixed using a diene rubber not modified with a bisalkylidene diaminoguanidine salt. It was at least confirmed.

表２中、配合処方の各成分は質量部を示す。

In Table 2, each component of the compounding prescription indicates part by mass.

  From Table 2, it was at least confirmed that the rubber compositions of the examples were excellent in low heat build-up and increased in tensile strength as compared with the rubber composition mixed without adding the bisalkylidene diaminoguanidine salt.

  This application includes a Japanese patent application filed with the Japan Patent Office on September 12, 2014 (Japanese Patent Application No. 2014-186073), and a Japanese patent application filed with the Japan Patent Office on September 12, 2014 ( Japanese Patent Application No. 2014-186075), the contents of which are incorporated herein by reference.

  The compound, modified rubber, and rubber composition according to the present invention can be used as materials for various tire members including tires.

Claims (15)

The compound represented by Formula (1) or Formula (2).

Wherein X is an acid forming a salt with the guanidine moiety, and R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl A group, and an alkenyl group (all of these groups include those having one or more substituents containing a sulfur atom, a nitrogen atom, or an oxygen atom), and at least one selected from the group consisting of hydrogen atoms is there.)

(In the formula, R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl group, and an alkenyl group (all of these groups are sulfur atoms, Including those having one or more substituents containing a nitrogen atom or an oxygen atom), and at least one selected from the group consisting of hydrogen atoms.) The compound of Claim 1 obtained by making the compound represented by Formula (3), and the compound represented by Formula (4) react.

(In the formula, X is an acid that forms a salt with the guanidine moiety of formula (3).)

(In the formula, R ¹ and R ² are each independently an alkyl group having 1 to 18 carbon atoms, a cycloalkyl group, an aryl group, an alkylaryl group, or an alkenyl group (all of these groups are a sulfur atom, a nitrogen atom) Or one having at least one substituent containing an oxygen atom) and at least one selected from the group consisting of hydrogen atoms.) R ¹ and R ² described in Formula (1) or Formula (2) are each independently selected from the group consisting of an alkyl group having 1 to 8 carbon atoms, an aryl group, an alkenyl group, and a hydrogen atom. The compound of Claim 1 or 2 which is at least 1 sort (s).   The compound as described in any one of Claims 1-3 whose melting | fusing point is 50-300 degreeC. The compound as described in any one of Claims 1-4 represented by either of Formula (5)-(10) and (12)-(14).

  A modified rubber (A) obtained by modifying at least one selected from the group consisting of natural rubber and synthetic rubber with the compound according to any one of claims 1 to 5.   At least one selected from the group consisting of the natural rubber and the synthetic rubber and the compound represented by the formula (1) or the formula (2) are mixed at a temperature of 20 to 180 ° C. and modified. The modified rubber (A) according to claim 6.   The modification | denaturation of Claim 6 or 7 whose usage-amount of the compound represented by said Formula (1) or Formula (2) is 0.01-10 mass% with respect to the total amount of a natural rubber and a synthetic rubber. Rubber (A).   A rubber composition comprising the modified rubber (A) according to any one of claims 6 to 8, a filler containing an inorganic filler (B), and a silane coupling agent (C).   The rubber composition according to claim 9, wherein the inorganic filler (B) is silica.   The rubber composition according to claim 9 or 10, wherein the filler contains carbon black. The compound represented by the formula (1) or the formula (2), at least one selected from the group consisting of the natural rubber and the synthetic rubber, a filler containing the inorganic filler (B), and the silane Obtained by mixing with a coupling agent (C),
A rubber composition containing the modified rubber (A) according to any one of claims 9 to 11.   The rubber composition according to claim 12, wherein the temperature during mixing is in the range of 20 to 180 ° C.   The usage-amount of the compound represented by said Formula (1) or Formula (2) is 0.01-10 mass% with respect to the total amount of the said natural rubber and the said synthetic rubber. Rubber composition.   A tire using the rubber composition according to any one of claims 9 to 14 for a tread of a tire member.