METHOD FOR PRODUCING TETRAFLUOROSULFANYL GROUP-CONTAINING ARYL COMPOUND

Abstract

The present invention is a method for producing a tetrafluorosulfanyl group-containing aryl compound, in which a thioaryl compound represented by General Formula (2) is subjected to a reaction by adding to an olefin compound represented by General Formula (3) in the presence of a radical initiator to synthesize a tetrafluorosulfanyl group-containing aryl compound represented by General Formula (1) [in the formula, A.sup.1 is an aryl group which may have a substituent, or a heteroaryl group which may have a substituent; and R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are each independently a hydrogen atom, a fluorine atom, or a chlorine atom, and two or more of R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are a fluorine atom].

##STR00001##

Claims

1. A method for producing a tetrafluorosulfanyl group-containing aryl compound, comprising: subjecting a thioaryl compound represented by General Formula (2) to a reaction by adding to an olefin compound represented by General Formula (3) in the presence of a radical initiator to synthesize a tetrafluorosulfanyl group-containing aryl compound represented by General Formula (1), ##STR00032## [in the formula, A.sup.1 is an aryl group which may have a substituent, or a heteroaryl group which may have a substituent] ##STR00033## [in the formula, R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are each independently a hydrogen atom, a fluorine atom, or a chlorine atom, provided that two or more of R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are a fluorine atom] ##STR00034## [in the formula, A.sup.1, R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are the same as above].

2. The method for producing a tetrafluorosulfanyl group-containing aryl compound according to claim 1, wherein A.sup.1 is an aryl which may have one or more kinds of substituents selected from the group consisting of a halogen atom, an alkyl group, an alkenyl group, an aryl group, an alkoxy group, a hydroxy group, a carboxy group, an acyl group, a cyano group, an amino group, and a nitro group.

3. The method for producing a tetrafluorosulfanyl group-containing aryl compound according to claim 1, wherein the reaction is carried out at ?40? C. to 130? C.

4. A tetrafluorosulfanyl group-containing aryl compound represented by General Formula (1), ##STR00035## [in the formula, A.sup.1 is an aryl group which may have a substituent, or a heteroaryl group which may have a substituent; and R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are each independently a hydrogen atom, a fluorine atom, or a chlorine atom, and two or more of R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are a fluorine atom].

Description

DESCRIPTION OF EMBODIMENTS

[0021] In the present invention and the present specification, C.sub.p1-p2 (p1 and p2 are each a positive integer satisfying p1<p2) means a group in which the number of carbon atoms is p1 to p2.

[0022] In the present invention and the present specification, a C.sub.1-6 alkyl group is an alkyl group having 1 to 6 carbon atoms, and it may be linear or may be branched. Examples of the C.sub.1-6 alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an isopentyl group, a neopentyl group, a tert-pentyl group, and a hexyl group.

[0023] In the present invention and the present specification, the term C.sub.1-6 alkoxy group refers to a group in which an oxygen atom is bonded to the bond terminal of a C.sub.1-6 alkyl group. The C.sub.1-6 alkoxy group may be linear or may be branched. Examples of the C.sub.1-6 alkoxy group include a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a tert-butoxy group, a pentyloxy group, and a hexyloxy group.

[0024] In the present invention and the present specification, the term C.sub.2-6 alkenyl group refers to a group in which at least one carbon-carbon bond of an alkyl group having 2 to 6 carbon atoms is an unsaturated bond. The C.sub.2-6 alkenyl group may be linear or may be branched. Examples of the C.sub.2-6 alkenyl group include a vinyl group, an allyl group, a butenyl group, a pentenyl group, and a hexenyl group.

[0025] In the present invention and the present specification, C.sub.2-7 acyl group refers to a group in which a hydrocarbon group moiety obtained by removing a carbonyl group from an acyl group is a C.sub.1-6 alkyl group, a C.sub.2-6 alkenyl group, an aryl group of a 5-membered ring or 6-membered ring, or a heteroaryl group of a 5-membered ring or 6-membered ring. The hydrocarbon group moiety of the acyl group may be linear or may be branched. Examples of the C.sub.2-7 acyl group include a formyl group, an acetyl group, a propanoyl group, a propenoyl group, and a benzoyl group.

[0026] In the present invention and the present specification, the term halogen atom refers to a fluorine atom, a chlorine atom, a bromine atom, or an iodine atom, and the term halogen atom other than a fluorine atom refers to a chlorine atom, a bromine atom, or an iodine atom. As an example of the halogen atom other than a fluorine atom, a chlorine atom or a bromine atom is preferable, and a chlorine atom is particularly preferable.

[0027] In addition, hereinafter, compound (n) means a compound represented by Formula (n).

<Addition Reaction Between SF.SUB.4.Cl Compound and Fluorine-Substituted Olefin>

[0028] In a method for producing a tetrafluorosulfanyl group-containing aryl compound (hereinafter, sometimes referred to as SF.sub.4-containing aryl compound) according to the present invention, the sulfur atom in the SF.sub.4Cl group in the SF.sub.4Cl group-containing aryl compound is added to a fluorine-substituted olefin. Specifically, a thioaryl compound represented by General Formula (2) is subjected to a reaction by adding to an olefin compound represented by General Formula (3) in the presence of a radical initiator. As a result, a tetrafluorosulfanyl group-containing aryl compound (1) having higher hydrophobicity than a SF.sub.5-containing aryl compound is obtained.

##STR00006##

[0029] In General Formula (2) and General Formula (1), A.sup.1 is an aryl group which may have a substituent, or a heteroaryl group which may have a substituent. The aryl group is not particularly limited. Examples thereof include a phenyl group, a naphthyl group, an anthryl group, and a 9-fluorenyl group, where a phenyl group is particularly preferable. The heteroaryl group is not particularly limited, and examples thereof include a pyridyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a pyrazolyl group, a quinolyl group, an isoquinolyl group, a pyrrolyl group, an imidazolyl group, an indolyl group, a furyl group, a benzofuryl group, a thienyl group, a benzothienyl group, an oxazolyl group, an isoxazolyl group, a thiazolyl group, and an isothiazolyl group.

[0030] The aryl group which may be substituted is a group in which one or more or a plurality of hydrogen atoms bonded to carbon atoms of an aryl group, preferably 1 to 3 hydrogen atoms, are substituted with other functional groups. Similarly, the heteroaryl group which may be substituted is a group in which one or more or a plurality of hydrogen atoms bonded to carbon atoms of a heteroaryl group, preferably 1 to 3 hydrogen atoms, are substituted with other functional groups. In a case where two or more substituents are contained, the substituents may be the same or different from each other.

[0031] The aryl group and heteroaryl group as A.sup.1 may have one or two or more substituents in addition to the sulfur atom for fluorination. Examples of the substituent include a halogen atom, an alkyl group, an alkenyl group, an alkoxy group, an aryl group, an acyl group, a hydroxy group, a carboxyl group, an alkyloxycarbonyl group, an aryloxycarbonyl group, a cyano group, and an amino group. The alkyl group is preferably a C.sub.1-6 alkyl group, the alkenyl group is preferably a C.sub.2-6 alkyl group, the alkoxy group is preferably a C.sub.1-6 alkoxy group, and the acyl group is preferably a C.sub.2-7 acyl group. The alkyloxycarbonyl group is preferably a group in which the alkyl group moiety is a C.sub.1-6 alkyl group, and more preferably a group in which the alkyl group moiety is a C.sub.1-3 alkyl group. The aryloxycarbonyl group is preferably a group in which the aryl group moiety is a phenyl group.

[0032] In General Formula (3), R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are each independently a hydrogen atom, a fluorine atom, or a chlorine atom. However, two or more of R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are a fluorine atom. Examples of the compound (3) include CF.sub.2?CF.sub.2, CF.sub.2?CFCl, CF.sub.2?CHF, CF.sub.2?CCl.sub.2, CF.sub.2?CHCl, CF.sub.2?CH.sub.2, CFCl?CFCl, CFCl?CHF, and CHF?CHF.

[0033] The amount of the thioaryl compound (2) that is added to a reaction system may be any amount that is equal to or larger than the stoichiometric amount thereof. In terms of reaction efficiency and cost, the amount of the thioaryl compound (2) to be used is preferably 1 to 10 equivalents and more preferably 1 to 6 equivalents of the olefin compound (3).

[0034] The addition reaction between the thioaryl compound (2) and the olefin compound (3) was carried out in the presence of a radical initiator. As the radical initiator, an initiator known in the related art can be used. Specifically, for example, an azo compound or a peroxide can be used as the radical initiator. The radical initiator to be used in the addition reaction between the thioaryl compound represented by General Formula (2) and the olefin compound represented by General Formula (3) preferably includes an azo compound.

[0035] Examples of the radical initiators as the azo compound include azobisisobutyronitrile (hereinafter, also referred to as AIBN), 2,2-azobis-2-methylbutyronitrile, 2,2-azobis-2,4-dimethylvaleronitrile (ADVN), 2,2-azobis-N-butyl-2-methylpropionamide, dimethyl-2,2-azobis-2-methylpropionamide, and 1,1-azobis-cyclohexane-1-carbonitrile. In terms of solubility in a reaction system, AIBN, 2,2-azobis-2-methylbutyronitrile, or 2,2-azobis-2,4-dimethylvaleronitrile is preferable.

[0036] Examples of the radical initiator as the peroxide include benzoyl peroxide, t-butyl peroxide, acetyl peroxide, diisopropyl peroxydicarbonate, t-butylperoxy-2-ethylhexanate, 2-hexyl-peroxy-2-ethylhexanate, and 1,1,3,3-tetramethylbutylperoxy-2-ethylhexanoate. In terms of easy control of the reaction, benzoyl peroxide, t-butyl peroxide, t-butylperoxy-2-ethylhexanate, or 2-hexyl-peroxy-2-ethylhexanate is preferable.

[0037] The addition reaction between the thioaryl compound (2) and the olefin compound (3) can be carried out in a solvent inert to the addition reaction. The inert solvent is not particularly limited; however, it is preferably an aprotic polar solvent. Examples of the aprotic polar solvent include acetonitrile (MeCN), N,N-dimethylformamide (DMF), N,N-dimethylacetamide, dimethyl sulfoxide (DMSO), tetrahydrofuran (THF), dichloromethane (DCM), 1,2-dichloroethane (DCE), and diethyl ether. The solvent to be used in the reaction may be a mixed solvent of two or more kinds of solvents.

[0038] In the addition reaction, a reaction solution obtained by mixing the thioaryl compound (2), the olefin compound (3), and a radical initiator in a reaction solvent is reacted at an appropriate temperature for an appropriate time. The addition reaction proceeds under mild conditions. For example, the reaction temperature is not particularly limited as long as the reaction solvent is liquid. The reaction can be carried out at ?40? C. to 130? C., preferably carried out at 0? C. to 80? C., and preferably carried out at 20? C. to 50? C., and it can also be carried out at room temperature (0? C. to 30? C.). For example, in a case where the addition reaction is carried out at 20? C. to 50? C. for less than 3 hours, the target tetrafluorosulfanyl group-containing aryl compound (1) can be obtained in an intrinsically quantitative yield.

EXAMPLES

[0039] Hereinafter, the present invention will be described in detail according to Examples; however, the present invention is not limited to these Examples.

[0040] The NMR apparatus used for the analysis in Examples and Comparative Examples is JNM-ECZ400S (400 MHz) manufactured by JEOL Ltd., and a reference value of tetramethylsilane is 0 PPM for .sup.1H NMR, and a reference value of C.sub.6F.sub.6 is ?162 PPM for .sup.19F NMR.

<Synthesis of Aryl Compound Containing Tetrafluorosulfanyl Group>

[0041] A tetrafluorosulfanyl group-containing aryl compound was synthesized according to the following synthetic procedure.

##STR00007##

[0042] Under a nitrogen atmosphere, a solution obtained by dissolving the compound (1) (0.20 mmol) and ADVN (10% by mole) in DCE (0.1 M) was stirred in a microwave vial (10 mL) and then cooled to 0? C. Next, tetrafluoroethylene (TFE) was added to the solution (1.0 atm) by bubbling. After carrying out stirring in an oil bath at 40? C. for 72 hours, insoluble solids were removed by filtration, and the filtrate was subjected to evaporation under reduced pressure. The obtained crude product was purified by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)) to obtain the desired compound (2).

Example 1

Synthesis of (2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)benzene

[0043] According to the procedure described above, (2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)benzene was obtained from (chlorotetrafluoro-?.sup.6-sulfanyl)benzene. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), (2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)benzene (0.024 g, yield: 37%) was obtained as colorless crystals.

##STR00008##

[0044] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.71-7.83 (m, 2H), 7.42-7.54 (m, 3H).

[0045] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 47.7 (m, 4F), ?67.9 (t, J=10.8 Hz, 2F), ?90.8 (m, 2F).

Example 2

Synthesis of 4-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)nitrobenzene

[0046] According to the procedure described above, 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)nitrobenzene was obtained from 4-(chlorotetrafluoro-?.sup.6-sulfanyl)nitrobenzene. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)nitrobenzene (0.040 g, yield: 55%) was obtained as colorless crystals.

##STR00009##

[0047] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 8.33 (d, J=8.7 Hz, 2H), 8.00 (d, J=9.2 Hz, 2H).

[0048] .sup.13C NMR (100 MHz, CDCl.sub.3) ? 159.4 (quint, J.sub.C-F=21.9 Hz), 149.2, 127.7 (quint, J.sub.C-F=4.8 Hz), 124.2, 122.1 (tt, J.sub.C-F=303.4, 35.6 Hz), 121.3 (ttquint, J.sub.C-F=312.1, 37.6, 36.6 Hz).

[0049] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 48.0 (m, 4F), ?68.1 (t, J=10.7 Hz, 2F), ?90.7 (m, 2F).

Example 3

Synthesis of 3-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)nitrobenzene

[0050] According to the procedure described above, 3-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)nitrobenzene was obtained from 3-(chlorotetrafluoro-?.sup.6-sulfanyl)nitrobenzene. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), 3-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)nitrobenzene (0.034 g, yield: 46%) was obtained as a colorless liquid.

##STR00010##

[0051] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 8.67 (s, 1H), 8.41 (d, J=8.2 Hz, 1H), 8.13 (d, J=8.2 Hz, 1H), 7.71 (t, J=8.2 Hz, 1H).

[0052] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 48.3 (m, 4F), ?68.1 (t, J=10.8 Hz, 2F), ?90.6 (m, 2F).

Example 4

Synthesis of 4-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)fluorobenzene

[0053] According to the procedure described above, 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)fluorobenzene was obtained from 4-(chlorotetrafluoro-?.sup.6-sulfanyl)fluorobenzene. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)fluorobenzene (0.035 g, yield: 51%) was obtained as a colorless liquid.

##STR00011##

[0054] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.77-7.82 (m, 2H), 7.11-7.16 (m, 2H).

[0055] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 49.0 (m, 4F), ?68.0 (t, J=10.8 Hz, 2F), ?90.7 (m, 2F).

Example 5

Synthesis of 3-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)fluorobenzene

[0056] According to the procedure described above, 3-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)fluorobenzene was obtained from 3-(chlorotetrafluoro-?.sup.6-sulfanyl)fluorobenzene. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), 3-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)fluorobenzene (0.012 g, yield: 18%) was obtained as a colorless liquid.

##STR00012##

[0057] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.58-7.61 (m, 1H), 7.50-7.55 (m, 1H), 7.42-7.49 (m, 1H), 7.20-7.26 (m, 1H).

[0058] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 48.0 (m, 4F), ?68.0 (t, J=10.8 Hz, 2F), ?90.8 (m, 2F).

Example 6

Synthesis of 2-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)fluorobenzene

[0059] According to the procedure described above, 2-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)fluorobenzene was obtained from 2-(chlorotetrafluoro-?.sup.6-sulfanyl)fluorobenzene. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), 2-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)fluorobenzene (0.009 g, yield: 13%) was obtained as a colorless liquid.

##STR00013##

[0060] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.79 (m, 1H), 7.51 (m, 1H), 7.19-7.26 (m, 2H).

[0061] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 49.0 (m, 4F), ?68.0 (t, J=10.8 Hz, 2F), ?90.7 (m, 2F).

Example 7

Synthesis of 4-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)chlorobenzene

[0062] According to the procedure described above, 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)chlorobenzene was obtained from 4-(chlorotetrafluoro-?.sup.6-sulfanyl)chlorobenzene. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)chlorobenzene (0.035 g, yield: 50%) was obtained as a colorless liquid.

##STR00014##

[0063] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.72 (d, J=9.1 Hz, 2H), 7.43 (d, J=9.1 Hz, 2H).

[0064] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 48.4 (m, 4F), ?68.0 (t, J=10.8 Hz, 2F), ?90.7 (m, 2F).

Example 8

Synthesis of 4-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)bromobenzene

[0065] According to the procedure described above, 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)bromobenzene was obtained from 4-(chlorotetrafluoro-?.sup.6-sulfanyl)bromobenzene. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)bromobenzene (0.019 g, yield: 24%) was obtained as a colorless liquid.

##STR00015##

[0066] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.65 (d, J=9.1 Hz, 2H), 7.60 (d, J=9.1 Hz, 2H).

[0067] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 48.3 (m, 4F), ?68.0 (t, J=10.8 Hz, 2F), ?90.8 (m, 2F).

Example 9

Synthesis of ethyl 4-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl) benzoate

[0068] According to the procedure described above, ethyl 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl) benzoate was obtained from ethyl 4-(chlorotetrafluoro-?.sup.6-sulfanyl) benzoate. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), ethyl 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl) benzoate (0.038 g, yield: 48%) was obtained as a colorless liquid.

##STR00016##

[0069] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 8.12 (d, J=8.7 Hz, 2H), 7.85 (d, J=9.0 Hz, 2H), 4.42 (q, J=7.0 Hz, 2H), 1.41 (d, J=7.1 Hz, 3H).

[0070] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 47.6 (m, 4F), ?68.0 (t, J=10.8 Hz, 2F), ?90.8 (m, 2F).

Example 10

Synthesis of 4-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)tert-butylbenzene

[0071] According to the procedure described above, 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)tert-butylbenzene was obtained from 4-(chlorotetrafluoro-?.sup.6-sulfanyl)tert-butylbenzene. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)tert-butylbenzene (0.014 g, yield: 18%) was obtained as a colorless liquid.

##STR00017##

[0072] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.70 (d, J=9.1 Hz, 2H), 7.45 (d, J=7.8 Hz, 2H), 1.34 (s, 9H).

[0073] .sup.19F NMR (376 MHz, CDCl.sub.3) ?48.2 (m, 4F), ?67.9 (t, J=10.8 Hz, 2F), ?90.8 (m, 2F).

Example 11

Synthesis of 2-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)-5-nitropyridine

[0074] According to the procedure described above, 2-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)-5-nitropyridine was obtained from 2-(chlorotetrafluoro-?.sup.6-sulfanyl)-5-nitropyridine. Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), 2-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)-5-nitropyridine (0.024 g, yield: 33%) was obtained as a colorless liquid.

##STR00018##

[0075] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 9.39 (d, J=2.7 Hz, 1H), 8.72 (m, 1H), 8.02 (d, J=8.7 Hz, 1H).

[0076] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 38.5 (m, 4F), ?68.3 (m, 2F), ?91.2 (m, 2F).

Synthesis Example 1

[0077] Under a nitrogen atmosphere, (2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)benzene (0.07 mmol), AIBN (50% by mole), and tris(trimethylsilyl)silane (3.0 equivalents) were dissolved in toluene (1.3 mL) in a glass vial (15 mL), and stirring was carried out in an oil bath at 100? C. for 1 hour. Thereafter, the solvent was evaporated under reduced pressure, and the obtained crude product was purified by flash silica gel column chromatography (n-hexane/EtOAc=9/1 (volume ratio)), whereby the desired (1,1,2,2-tetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)benzene (0.014 g, yield: 40%) was obtained as a colorless liquid.

##STR00019##

[0078] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.76-7.81 (m, 2H), 7.44-7.51 (m, 3H), 6.18 (m, 1H).

[0079] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 42.7 (m, 4F), ?98.0 (m, 2F), ?134.3 (m, 2F).

Example 12

Synthesis of 4-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)aniline

[0080] To a solution obtained by dissolving 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)nitrobenzene (0.98 mmol) in ethanol (20 mL), iron (11 equivalents) and a saturated aqueous ammonium chloride solution (5 mL) were added, and stirring was carried out in an oil bath at 80? C. for 2 hours. Thereafter, insoluble solids were removed by filtration through celite, and the filtrate was subjected to evaporation under reduced pressure. The obtained crude product was dissolved in ethyl acetate and washed with water, and the aqueous layer was extracted twice with ethyl acetate. Then, the combined organic extracts were dried with sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained crude product was purified by flash silica gel column chromatography (n-hexane/EtOAc=4/1 (volume ratio)), whereby the desired 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)aniline (0.311 g, yield: 95%) was obtained as a pale yellow liquid.

##STR00020##

[0081] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.55 (d, J=8.7 Hz, 2H), 6.58 (d, J=9.1 Hz, 2H), 3.97 (br, 2H)

[0082] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 49.5 (m, 4F), ?67.9 (t, J=10.8 Hz, 2F), ?90.7 (m, 2F).

Example 13

[0083] A tetrafluorosulfanyl group-containing aryl compound was synthesized according to the following synthetic procedure.

##STR00021##

[0084] Under a nitrogen atmosphere, a solution obtained by dissolving the compound (1) and ADVN (10% by mole) in EtOAc (0.25 M) was stirred in a microwave vial (25 mL) and then cooled to 0? C. Next, tetrafluoroethylene (TFE) was added to the solution (1.0 atm) by bubbling. After carrying out stirring in an oil bath at 40? C. for 72 hours, insoluble solids were removed by filtration, and the filtrate was subjected to evaporation under reduced pressure. The obtained crude product was purified by flash silica gel column chromatography (n-hexane/EtOAc) to obtain the desired compound (2).

(1) Synthesis of 4-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)phenyl acetate

[0085] According to the procedure described above, 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)phenyl acetate was obtained from 4-(chlorotetrafluoro-?.sup.6-sulfanyl)phenyl acetate (0.6 mmol). Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=19/1 (volume ratio)), 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)phenyl acetate (0.164 g, yield: 72%) was obtained as colorless crystals.

##STR00022##

[0086] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.80 (d, J=9.2 Hz, 2H), 7.19 (d, J=8.7 Hz, 2H), 2.32 (s, 3H).

[0087] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 49.2 (m, 4F), ?67.4 (t, J=11.6 Hz, 2F), ?90.2 (m, 2F).

(2) Synthesis of 2-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)pyridine

[0088] According to the procedure described above, 2-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)pyridine was obtained from 2-(chlorotetrafluoro-?.sup.6-sulfanyl)pyridine (1.0 mmol). Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=4/1 (volume ratio)), 2-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)pyridine (0.230 g, yield: 72%) was obtained as a colorless liquid.

##STR00023##

[0089] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 8.57 (d, J=4.1 Hz, 1H), 7.92 (t, J=7.3 Hz, 1H), 7.77 (d, J=8.2 Hz, 1H), 7.49 (dd, J=7.3, 4.6 Hz, 1H).

[0090] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 38.0 (m, 4F), ?67.5 (m, 2F), ?90.7 (m, 2F).

(3) Synthesis of 2-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)pyrimidine

[0091] According to the procedure described above, 2-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)pyrimidine was obtained from 2-(chlorotetrafluoro-?.sup.6-sulfanyl)pyrimidine (0.5 mmol). Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=1/1 (volume ratio)), 2-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)pyrimidine (0.129 g, yield: 80%) was obtained as a colorless liquid.

##STR00024##

[0092] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 8.93 (d, J=4.6 Hz, 2H), 7.57 (t, J=4.6 Hz, 1H).

[0093] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 33.7 (m, 4F), ?67.5 (m, 2F), ?91.1 (m, 2F).

(4) Synthesis of 1-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)-2,3,4,5,6-pentafluorobenzene

[0094] According to the procedure described above, 1-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)-2,3,4,5,6-pentafluorobenzene was obtained from 1-(chlorotetrafluoro-?.sup.6-sulfanyl)-2,3,4,5,6-pentafluorobenzene (0.5 mmol, a mixture of cis form:trans form=2:3). Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=19/1 (volume ratio)), 1-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)-2,3,4,5,6-pentafluorobenzene (0.072 g, yield: 58%) was obtained as a colorless liquid.

##STR00025##

[0095] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 59.2 (m, 4F), ?67.9 (t, J=10.8 Hz, 2F), ?91.4 (m, 2F), ?132.4 (m, 2F), ?146.8 (m, 1F), ?159.0 (m, 2F).

Example 14

[0096] A tetrafluorosulfanyl group-containing aryl compound was synthesized according to the following synthetic procedure.

##STR00026##

[0097] Under a nitrogen atmosphere, a solution obtained by dissolving the compound (1) and AIBN (10% by mole) in EtOAc (0.25 M) was stirred in a microwave vial (25 mL) and then cooled to 0? C. Next, tetrafluoroethylene (TFE) was added to the solution (1.0 atm) by bubbling. After carrying out stirring in an oil bath at 60? C. for 48 hours, insoluble solids were removed by filtration, and the filtrate was subjected to evaporation under reduced pressure. The obtained crude product was purified by flash silica gel column chromatography (n-hexane/EtOAc) to obtain the desired compound (2).

(1) Synthesis of 4-(2-chlorotetrafluoroethyltetrafluoro-?.SUP.6.-sulfanyl)toluene

[0098] According to the procedure described above, 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)toluene was obtained from 4-(chlorotetrafluoro-?.sup.6-sulfanyl)toluene (1.0 mmol). Following purification carried out by flash silica gel column chromatography (n-hexane/EtOAc=19/1 (volume ratio)), 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)toluene (0.225 g, yield: 67%) was obtained as colorless crystals.

##STR00027##

[0099] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.66 (d, J=8.7 Hz, 2H), 7.24 (d, J=8.2 Hz, 2H), 2.40 (s, 3H).

[0100] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 48.8 (m, 4F), ?67.3 (t, J=11.6 Hz, 2F), ?90.2 (m, 2F).

Example 15

[0101] A solution obtained by dissolving 2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanylbenzene (0.20 mmol) and ADVN (10% by mole) in EtOAc (0.05M) was frozen with liquid nitrogen and degassed under reduced pressure. Next, tetrafluoroethylene (TFE) was added thereto to 1.1 MPa while stirring the solution at 0? C. Stirring was carried out in an oil bath at 40? C. for 24 hours to obtain the desired compound (3) in a yield of 42% as determined by NMR. Compound (3) satisfying 1?n?7 was detected in the GC/MS analysis.

##STR00028##

[0102] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 48.3-47.3 (m, 4F), ?67.9-?67.3 (m, 2F), ?90.5-?90.2 (m, 2F), ?121.5-?118.4 (m, 4 (n?1)F).

Example 16

[0103] To a solution obtained by dissolving 3-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)nitrobenzene (0.75 mmol) in ethanol (15 mL), iron (10 equivalents) and a saturated aqueous ammonium chloride solution (3.7 mL) were added, and stirring was carried out in an oil bath at 80? C. for 2 hours. Thereafter, insoluble solids were removed by filtration through celite, and the filtrate was subjected to evaporation under reduced pressure. The obtained crude product was dissolved in ethyl acetate and washed with water, and the aqueous layer was extracted twice with ethyl acetate. Then, the combined organic extracts were dried with sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained crude product was purified by flash silica gel column chromatography (n-hexane/EtOAc=4/1 (volume ratio)), whereby the desired 3-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)aniline (0.209 g, yield: 83%) was obtained as a pale yellow liquid.

##STR00029##

[0104] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.20 (t, J=7.8 Hz, 1H), 7.14 (d, J=8.2 Hz, 1H), 7.07 (t, J=2.0 Hz, 1H), 6.76 (d, J=7.8 Hz, 1H), 3.84 (br, 2H).

[0105] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 48.0 (m, 4F), ?67.3 (t, J=10.0 Hz, 2F), ?90.3 (m, 2F).

Example 17

[0106] Under a nitrogen atmosphere, 3-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)aniline (0.40 mmol), 1,1-azobis(cyclohexane-1-carbonitrile) (V-40) (15% by mole), and tris(trimethylsilyl)silane (5.0 equivalents) were dissolved in toluene (2.0 mL) in a microwave vial (10 mL), and stirring was carried out in an oil bath at 100? C. for 2 hours. Thereafter, the solvent was evaporated under reduced pressure, the obtained crude product was dissolved together with dimethylcarbamoyl chloride (6.0 equivalents) and triethylamine (2.0 equivalents) in tetrahydrofuran (2.0 equivalents), and then stirring was carried out at room temperature for 20 hours. The obtained crude product was extracted three times with a mixed solvent of ethyl acetate/hexane and then washed three times with each of a saturated aqueous citric acid solution and a saturated aqueous sodium chloride solution. The obtained organic extract was dried with sodium sulfate, the solvent was evaporated under reduced pressure, and then purification was carried out by flash silica gel column chromatography (n-hexane/EtOAc=2/1 (volume ratio)) to obtain the desired N,N-dimethyl-N-[3-(1,1,2,2-tetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)phenyl]urea (0.045 g, yield: 30%) as a pale yellow liquid.

##STR00030##

[0107] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.83 (m, 1H), 7.52 (m, 1H), 7.38 (m, 1H), 7.30 (m, 1H), 6.70 (br, 1H), 6.14 (m, 1H), 3.00 (s, 6H).

[0108] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 43.4 (m, 4F), ?97.5 (t, J=10.0 Hz, 2F), ?133.6 (d, J=55.2 Hz, 2F).

Example 18

[0109] 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)bromobenzene (0.50 mmol) was dissolved together with tetrakis(triphenylphosphine) palladium(0) (3% by mole) in dimethoxyethane (1.0 mL), and stirring was carried out for 10 minutes. Thereafter, a saturated ethanol solution of phenylboronic acid (1.1 equivalents) and a saturated aqueous solution of sodium carbonate (2.0 equivalents) was added thereto, and stirring was carried out in an oil bath at 80? C. for 18 hours. Thereafter, insoluble solids were removed by filtration, and the filtrate was dissolved in ethyl acetate and then washed three times with a saturated aqueous sodium chloride solution. The obtained organic extract was dried with sodium sulfate, and the solvent was evaporated under reduced pressure. Then, purification was carried out by flash silica gel column chromatography (n-hexane/EtOAc=19/1 (volume ratio)) to obtain the desired 4-(2-chlorotetrafluoroethyltetrafluoro-?.sup.6-sulfanyl)biphenyl (0.182 g, yield: 92%) was obtained as a colorless solid.

##STR00031##

[0110] .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.87 (d, J=8.2 Hz, 2H), 7.66 (d, J=8.2 Hz, 2H), 7.60 (d, J=8.2 Hz, 2H), 7.50 (t, J=7.8 Hz, 2H), 7.44 (t, J=7.8 Hz, 1H).

[0111] .sup.19F NMR (376 MHz, CDCl.sub.3) ? 48.9 (m, 4F), ?67.3 (t, J=11.6 Hz, 2F), ?90.1 (m, 2F).

INDUSTRIAL APPLICABILITY

[0112] The present invention provides a manufacturing method that makes it possible to synthesize an SF.sub.4-containing aryl compound in a single step under relatively mild conditions. The present invention is useful for introducing an SF.sub.4 group into active ingredients of pharmaceutical drugs or agricultural chemicals or in organic materials.