JP2015059097A - Method of producing perfluoro branched alkylaniline - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a method of producing a perfluoro branched alkylaniline inexpensively at a high yield.SOLUTION: A method of producing a perfluoro branched alkylaniline is characterized by reacting a perfluoro branched alkyl bromide represented by the specified general formula (I), where Rf represents a C3-6 branched perfluoroalkyl group, with an aniline represented by the specified general formula (II), where Rto Rrepresent hydrogen atoms or the like, in the presence of a base and in the presence of a reductant or light irradiation, and at least in the presence of a polar solvent whose dielectric constant at 25°C is 5 or greater.

Description

  The present invention relates to a method for producing perfluoro branched alkylanilines which are useful intermediates.

  Perfluoro branched alkyl anilines are known as useful intermediates. Perfluoro branched alkyl anilines are used as an intermediate for producing, for example, agricultural chemicals or medicines.

  As a method for producing perfluoro linear alkylanilines, for example, the method shown in Non-Patent Document 1 is known.

  As a method for producing a perfluoro branched alkyl aniline, for example, a method of reacting a perfluoro branched alkyl iodide with an aniline is known (Patent Document 1). However, this method has a problem that perfluoro branched alkyl iodide used as a raw material is very expensive.

  Further, as another method for producing perfluoro branched alkyl anilines, a method of reacting relatively inexpensive perfluoro branched alkyl chloride or perfluoro branched alkyl bromide with anilines in an organic solvent two-phase system is known. (Patent Documents 2 and 3). However, these methods have a problem that the yield of perfluoro branched alkyl anilines which are target products is not sufficient.

JP 2001-122836 A JP 2003-335735 A JP 2004-161768 A

Xiao-Ting Huang, 7 others, Journal of Fluorine Chemistry, 2001, 111, pp. 107-113

  The present invention has been made in view of the current state of the prior art described above, and its main object is to provide a method for producing perfluoro branched alkylanilines at a relatively low cost and in a high yield. is there.

  The inventors of the present invention have intensively studied to achieve the above-described object. As a result, an aniline and a relatively inexpensive perfluoro branched alkyl bromide are polar having a relative dielectric constant of 30 or more at 25 ° C. in the presence of a base and in the presence of a reducing agent or under light irradiation. By reacting in the presence of a solvent, it was found that perfluoro-branched alkylanilines, which are target products, were obtained in high yield, and the present invention was completed here.

That is, the present invention provides the following embodiments.
Item 1.
Perfluoro branched alkyl bromide represented by the following general formula (I)

(Wherein Rf represents a branched perfluoroalkyl group having 3 to 6 carbon atoms) and anilines represented by the following general formula (II)

(In formula, R < ¹ > -R < ⁶ > is the same or different, and is a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, or carbon. A haloalkoxy group of the number 1 to ⁶ and at least one of R ¹ and R ² , R ³ and R ⁴ , and R ⁵ and R ⁶ may form a ring),
In the presence of a base and in the presence of a reducing agent or light irradiation,
The reaction is performed in the presence of a polar solvent having a relative dielectric constant of 5 or more at 25 ° C., at least,
Perfluoro branched alkylanilines represented by the following general formula (III)

(The definitions in the formula are as described above.)
Manufacturing method.
Item 2.
Item _2. The production method according to Item 1, wherein the perfluoro branched alkyl bromide is perfluoroisopropyl bromide (CF ₃ ) ₂ CFBr.
Item 3.
Item 3. The production method according to Item 1 or 2, wherein the aniline is 2-methylaniline.
Item 4.
Item 4. The production method according to any one of Items 1 to 3, wherein the polar solvent is at least one polar solvent selected from the group consisting of dimethyl sulfoxide, N, N-dimethylformamide, and acetonitrile.
Item 5.
Item 5. The production method according to any one of Items 1 to 4, wherein the base is at least one base selected from the group consisting of alkali metal salts, alkaline earth metal salts, ammonium salts, amines, and heterocyclic compounds. .
Item 6.
Item 6. The production method according to any one of Items 1 to 5, wherein the reducing agent is dithionite.

  By using the production method of the present invention, it is possible to obtain perfluoro branched alkyl anilines which are target products in high yield while using relatively inexpensive reaction raw materials.

  Hereinafter, the method of the present invention will be specifically described.

1. Perfluoro branched alkyl anilines The present invention is a method for producing perfluoro branched alkyl anilines represented by the following general formula (III).

(In the formula, Rf represents a branched perfluoroalkyl group having 3 to 6 carbon atoms, and R ^{1 to} R ⁶ are the same or different and are a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, carbon A haloalkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms or a haloalkoxy group having 1 to 6 carbon atoms, and at least ^one of R ¹ and R ² , R ³ and R ⁴ , and R ⁵ and R ⁶ ; A set may form a ring.)

  In the present invention, the halogen atom represents a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

  Moreover, in this invention, an alkyl group represents the linear or branched alkyl group which may have substitution.

  Specific examples of the perfluoro branched alkylanilines represented by the general formula (III) include 2-methyl-4-heptafluoroisopropylaniline represented by the following general formula (IV). This compound is useful as an intermediate in the production of fulvendiamide used as an insecticide.

2. Perfluoro branched alkyl bromide In the production method of the present invention, the perfluoro branched alkyl bromide used as a raw material is represented by the following general formula (I).

(In the formula, Rf represents a branched perfluoroalkyl group having 3 to 6 carbon atoms.)
As the perfluoro branched alkyl bromide represented by the above general formula (I), those having Rf of 3 to 5 carbon atoms are preferred, those having Rf of 3 to 4 carbon atoms are more preferred, and perfluoroisopropyl bromide (CF ₃ ) ₂ CFBr is more preferred.

  Although the equivalent of the perfluoro branched alkyl bromide used as a raw material in the production method of the present invention is not particularly limited, it can usually be 1.0 to 2.0 equivalents relative to 1 equivalent of anilines as a raw material described later. , Preferably 1.2 to 1.5 equivalents.

3. Anilines The anilines used as raw materials in the production method of the present invention are represented by the following general formula (II).

(In formula, R < ¹ > -R < ⁶ > is the same or different, and is a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, or carbon. A haloalkoxy group represented by formulas ^{1 to 6} and at least one of R ¹ and R ² , R ³ and R ⁴ , and R ⁵ and R ⁶ may form a ring.

The anilines represented by the general formula (II) are the same or different with respect to R ^{1 to} R ² , and are a hydrogen atom, a halogen atom, an alkyl group having 1 to 3 carbon atoms, or a haloalkyl having 1 to 3 carbon atoms. What is a group, a C1-C3 alkoxy group, or a C1-C3 haloalkoxy group is preferable.

As the anilines represented by the general formula (II), R ^{1 to} R ² are the same or different and more are hydrogen atoms, halogen atoms, methyl groups, halomethyl groups, methoxy groups, or halomethoxy groups. Preferably, all are hydrogen atoms.

As anilines represented by the general formula (II), regarding R ³ , an alkyl group having 1 to 3 carbon atoms, a haloalkyl group having 1 to 3 carbon atoms, an alkoxy group having 1 to 3 carbon atoms, or 1 carbon atom. Those that are ˜3 haloalkoxy groups are preferred.

As the anilines represented by the above general formula (II), R ³ is preferably a methyl group, a halomethyl group, a methoxy group or a halomethoxy group, more preferably a methyl group.

As anilines represented by the above general formula (II), R ^{4 to} R ⁶ are the same or different and are a hydrogen atom, a halogen atom, an alkyl group having 1 to 3 carbon atoms, or a haloalkyl having 1 to 3 carbon atoms. What is a group, a C1-C3 alkoxy group, or a C1-C3 haloalkoxy group is preferable.

As anilines represented by the above general formula (II), R ^{4 to} R ⁶ are the same or different and more are hydrogen atoms, halogen atoms, methyl groups, halomethyl groups, methoxy groups or halomethoxy groups. Preferably, all are hydrogen atoms.

As anilines represented by the general formula (II), for R ^{3 to} R ⁶ , R ³ is an alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, or an alkyl group having 1 to 6 carbon atoms. An alkoxy group or a haloalkoxy group having 1 to 6 carbon atoms in which R ^{4 to} R ⁶ are all hydrogen atoms is particularly preferable. Among these, R ³ is an alkyl group having 1 to 3 carbon atoms, a haloalkyl group having 1 to 3 carbon atoms, an alkoxy group having 1 to 3 carbon atoms, or a haloalkoxy group having 1 to 3 carbon atoms, and R ^{4 to} R More preferably, ⁶ is a hydrogen atom, R ³ is a methyl group, a halomethyl group, a methoxy group, or a halomethoxy group, and R ^{4 to} R ⁶ are all preferably a hydrogen atom, and R ³ is Most preferred is a methyl group and R ^{4 to} R ⁶ are all hydrogen atoms.

  Specific examples of the anilines represented by the general formula (II) include 2-methyl-aniline represented by the following general formula (V).

4). The base is not particularly limited as long as the effects of the present invention can be obtained, and examples thereof include alkali metal salts, alkaline earth metal salts, ammonium salts, amines, and heterocyclic compounds.

  Examples of the alkali metal salt and alkaline earth metal salt include hydroxides, acetates, phosphates, hydrogen phosphates, carbonates and hydrogen carbonates of alkali metals and alkaline earth metals. Specific examples of the alkali metal salt and the alkaline earth metal salt include sodium hydroxide, potassium hydroxide, sodium acetate, potassium acetate, calcium acetate, sodium carbonate, potassium carbonate, potassium hydrogen carbonate, and sodium hydrogen carbonate.

  Specific examples of the ammonium salt include ammonium acetate and ammonium carbonate.

  Specific examples of the amine include trimethylamine, triethylamine, tributylamine, diisopropylethylamine, tetramethylguanidine, N, N-dimethylaniline, diazabicyclooctane (DABCO), diazabicyclononene (DBC), diazabicycloundecene ( DBU), N-methylpiperidine, piperidine and the like.

  Specific examples of the heterocyclic compound include pyridine, 2-N, N-dimethylaminopyridine, 3-N, N-dimethylaminopyridine and 4-N, N-dimethylaminopyridine.

  As the base, these may be used alone or in combination of two or more.

  As the base, alkali metal hydroxides, alkali metal carbonates and alkali metal hydrogen carbonates are preferable, and alkali metal hydrogen carbonates are more preferable. Specific examples of the alkali metal hydrogen carbonate include sodium hydrogen carbonate.

  The amount of the base used is not particularly limited as long as the effect of the present invention can be obtained, but is usually 0.01 to 3 equivalents relative to anilines 1 as a reaction raw material, preferably 1.0 to 2. 0 equivalents.

5. The reducing agent is not particularly limited as long as energy necessary for starting the reaction is supplied by using the reducing agent. For example, a suitable amount of dithionite or the like can be used.

  Specific examples of dithionite include sodium dithionite and potassium dithionite.

  The amount of the reducing agent used is not particularly limited as long as the effect of the present invention can be obtained, but is usually 0.01 to 3 equivalents, preferably 0.1 to 2 with respect to anilines 1 as a reaction raw material. It is equivalent, More preferably, it is 1-2 equivalent, and 1.5 equivalent etc. are mentioned as a specific example.

6). The light irradiation light irradiation is not particularly limited as long as energy necessary for starting the reaction is supplied, and for example, irradiation can be performed under appropriate conditions using a high-pressure mercury lamp or the like as a light source.

  The reducing agent and light irradiation are both used for the purpose of supplying energy necessary for the start of the reaction, and either one of them may be used or both may be used together as necessary. Good.

7). Polar solvent A polar solvent is a solvent having a relative dielectric constant of 5 or more at 25 ° C. By carrying out the reaction in the presence of at least such a polar solvent, the perfluoro branched alkylanilines that are target products can be obtained in high yield.

  As the polar solvent, a polar solvent having a relative dielectric constant of 5 or more at 25 ° C. may be used alone, or two or more polar solvents having a relative dielectric constant of 5 or more at 25 ° C. may be used in combination. Also good.

  In the case of using one kind of polar solvent, it is preferable in terms of the yield of the target product that the relative dielectric constant at 25 ° C. alone is 30 to 50. When two or more kinds are mixed and used, in order to improve the yield of the target product, polar solvents each having a relative dielectric constant at 25 ° C. of 30 to 50 can be mixed and used.

  As the polar solvent, those having a relative dielectric constant corresponding to the above can be used alone and are not particularly limited. Specific examples of such a solvent include dimethyl sulfoxide (relative dielectric constant 47 at 25 ° C .; Similarly, the parentheses indicate relative permittivity at 25 ° C.), N, N-dimethylformamide (38), acetonitrile (37), methanol (24), sulfolane (42) and N-methylpyrrolidone (33) Etc. Further, polar solvents having a relative dielectric constant within the above range can be used in combination.

  As the polar solvent, dimethyl sulfoxide, N, N-dimethylformamide and acetonitrile are preferable in that side reactions are suppressed.

  As the polar solvent, dimethyl sulfoxide is particularly preferable.

  In addition to the polar solvent of the present invention, a solvent having a relative dielectric constant at 25 ° C. outside the range of 30 or more and 50 or less is added as an auxiliary solvent within the range of not impairing the effects of the present invention. Can do. By using the auxiliary solvent in combination, an effect of facilitating post-treatment after the reaction can be expected. Specific examples of co-solvents include aliphatic or aromatic, optionally halogenated hydrocarbons such as benzine fraction, benzene, toluene, xylene, chlorobenzene, dichlorobenzene, petroleum ether, hexane, cyclohexane, dichloromethane, chloroform or Examples include carbon tetrachloride, ether, ketone and ester. Specific examples of the ether include diethyl ether, diisopropyl ether, t-butyl methyl ether and cyclopentyl methyl ether. Specific examples of the ketone include cyclohexanone, butanone, methyl isobutyl ketone, and the like. Specific examples of the ester include methyl acetate and ethyl acetate. The amount of the auxiliary solvent can be appropriately adjusted. When the polar solvent of the present invention is 1 part by weight, usually 5 to 100 parts by weight of the auxiliary solvent can be used in combination.

8). Other Reaction Conditions The reaction temperature can be appropriately set within a range where the lower limit is 25 ° C. and the boiling point is the reaction condition of the polar solvent using the upper limit. 25-80 degreeC is preferable on industrial production.

  The reaction pressure is not particularly limited, but is usually from atmospheric pressure to 2 MPa (gauge pressure).

  Although reaction time is not specifically limited, Usually, it is 60 to 180 minutes.

9. After completion of the post-treatment and separation / purification reaction, the target product is subjected to post-treatment such as salt removal, polar solvent distillation, extraction and concentration of the crude product, if necessary. Certain perfluoro branched alkyl anilines can be isolated. Although it does not specifically limit, Specifically, it can operate as follows, for example.

  The salt can be removed by filtration after precipitation. If the salt is not removed, the final product cannot be isolated well at the end. For example, a nonpolar solvent (for example, ethyl acetate or the like) may be introduced into the reaction system and then stirred to precipitate a salt, which may be removed by filtration under reduced pressure. The nonpolar solvent can be removed from the filtrate thus obtained by distillation.

  The method for distilling off the polar solvent is not particularly limited. For example, after introducing a stabilizer (for example, potassium carbonate) if necessary, the polar solvent is distilled off under predetermined conditions (for example, 80 ° C./10 mmHg). And the like.

  Extraction of the target product is not particularly limited, but can be performed as follows, for example. After distilling off the polar solvent, an extraction solvent (such as ethyl acetate) and water are introduced, and after stirring, the two layers are separated, and the aqueous layer is removed. Furthermore, you may wash | clean as needed. The washing is not particularly limited, but can be performed using, for example, water or, if necessary, 5% aqueous hydrochloric acid. It can wash | clean by introduce | transducing the aqueous solution used for washing | cleaning, making it separate into two layers, and removing an aqueous layer. The cleaning may be performed a plurality of times, and in this case, the cleaning may be performed using an aqueous solution different from that used in the previous cleaning. Finally, the extraction solvent can be taken out, the solvent can be distilled off, and the target product can be isolated by simple distillation.

  The isolated target product may be further purified according to a conventional method, if necessary.

  EXAMPLES Hereinafter, although an Example and a comparative example are given and this invention is demonstrated further in detail, this invention is not limited to these Examples.

Example 1
The following reaction was performed as follows.

Toluidine (0.717 g), Na ₂ S ₂ O ₄ (1.75 g), NaHCO ₃ (0.84 g) and DMSO (7 ml) were charged into a stainless steel autoclave having an internal volume of 30 ml. The autoclave lid was closed, and N ₂ was sealed with 0.5 MPa, and it was confirmed that there was no leakage. After confirmation, the pressure was released, the Rf-Br cylinder and the reactor were connected, and 2 g of Rf-Br was charged. The temperature was adjusted so that the internal temperature became 70 ° C., and the mixture was stirred for 4 hours.

After stirring for 4 hours, CO ₂ produced as a by-product was purged and the autoclave was opened. AcOEt (30 ml) was introduced and stirred for 15 min to precipitate the salt. The precipitated salt was filtered under reduced pressure, and AcOEt was distilled off from the filtrate using an evaporator. Thereafter, 0.2 g of K ₂ CO ₃ was added, and DMSO was distilled off at 80 ° C./10 mmHg.

AcOEt (30 ml) and H ₂ O (30 ml) were introduced, and the mixture was stirred for 30 minutes and separated into two layers. After removing the aqueous layer, it was washed with 5% aqueous hydrochloric acid (30 ml) and separated into two layers. Further, the aqueous layer was removed, washed with water (30 ml), and after separation of the two layers, the aqueous layer was removed.

  AcOEt was distilled off from the obtained organic layer, and then the target product (the above RFA) was simply distilled (100 ° C./10 mmHg).

  The yield was 1.36 g, and the isolated yield was 75%.

Claims (6)

Perfluoro branched alkyl bromide represented by the following general formula (I)

(Wherein Rf represents a branched perfluoroalkyl group having 3 to 6 carbon atoms) and anilines represented by the following general formula (II)

(In formula, R < ¹ > -R < ⁶ > is the same or different, and is a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, or carbon. A haloalkoxy group represented by formulas 1 to 6).
In the presence of a base and in the presence of a reducing agent or light irradiation,
The reaction is performed in the presence of a polar solvent having a relative dielectric constant of 5 or more at 25 ° C., at least,
Perfluoro branched alkylanilines represented by the following general formula (III)

(The definitions in the formula are as described above.)
Manufacturing method. The production method according to claim 1, wherein the perfluoro branched alkyl bromide is perfluoroisopropyl bromide (CF ₃ ) ₂ CFBr. The production method according to claim 1 or 2, wherein the aniline is 2-methylaniline. The production method according to any one of claims 1 to 3, wherein the polar solvent is at least one polar solvent selected from the group consisting of dimethyl sulfoxide, N, N-dimethylformamide, and acetonitrile. The production according to any one of claims 1 to 4, wherein the base is at least one base selected from the group consisting of alkali metal salts, alkaline earth metal salts, ammonium salts, amines and heterocyclic compounds. Method. The manufacturing method as described in any one of Claims 1-5 whose said reducing agent is a dithionite.