USRE35177E - N-fluoropyridinium salt and process for preparing same - Google Patents

N-fluoropyridinium salt and process for preparing same Download PDF

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USRE35177E
USRE35177E US08/197,711 US19771194A USRE35177E US RE35177 E USRE35177 E US RE35177E US 19771194 A US19771194 A US 19771194A US RE35177 E USRE35177 E US RE35177E
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carbon atoms
hydrogen
acid
pyridine
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Teruo Umemoto
Kyoichi Tomita
Kosuke Kawada
Ginjiro Tomizawa
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Taiheiyo Cement Corp
Sagami Chemical Research Institute
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Chichibu Onoda Cement Corp
Sagami Chemical Research Institute
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Definitions

  • the present invention relates to a N-fluoropyridinium salt and a process for preparing same.
  • the N-fluoropyridinium salts according to the present invention are very useful as a fluorine atom introducing agent as seen from the examples 66-133 hereinafter illustrated.
  • the salts according to the invention have a widespread use because of their high reactivity with a wide variety of compounds and selectivity for any desired products.
  • said salt can be used for the preparation of 3-fluoro-4-hydroxyphenlacetic acid which is useful as a thyroid inhibitor by reacting the former with p-hydroxyphenylacetate followed by a common hydrolysis reaction as illustrated in examples 79 to 82 referred to hereinafter.
  • fluorine compounds are significantly distinguished from chlorine compounds, bromine compounds, and iodine compounds in their physical properties and reactivities, because fluorine atom have characteristics such as very high electronegativity, high ionization energy, extremely high bonding ability with other atoms, small Van der Waals diameter, lack of a d-electron orbit and the like (N. Ishikawa & Y. Kobayashi; FLUORINE COMPOUNDS; THEIR CHEMISTRY AND APPLICATIONS; KodanshaSchientific, pp. 69-70. 1979). Therefore, fluorination reactions naturally have significantly different aspects from other halogenation reactions such as chlorinations, brominations and iodinations.
  • F 2 complex can be used as a fluorine atom-introducing agent, but it can only offer low total yield of fluorination reactions [see, Z. Chem., 12, 292 (1972)] and moreover, said complex is highly hygroscopic and thermally unstable so that explosions may break out at above -2°C. [Z. Chem., 5, 64 (1965)]. From the above, it can hardly be said that the complex is a useful fluorinating agent. Recently, N-fluoro-N-alkylarenesulfoneamide have been reported as fluorine atom-introducing agents, but these compounds are low in reactivity and only effective for particular reaction species (negatively charged carbon ions) [J. Amer. Chem. Soc. 106, 452 (1984)]. Therefore, a strong need exists for the development of highly satisfactory fluorine atom-introducing agents.
  • the compounds according to the present invention have high reactivity with a variety of compounds and high selectivity for any desired compounds, which allows the compounds to be very useful for the synthesis of a variety of fluorine-containing compounds in a shortened process.
  • a thyroid inhibitor, 3-fluoro4-hydroxy-phenylacetic acid could easily be prepared from p-hydorxyphenylacetate available industrially (see, Examples 79-82 hereinafter described).
  • the present invention relates to a N-fluoropyridiuium salt represented by the formula: ##STR1## wherein R 1 , R 2 , R 3 , R 4 and R 5 represent a hydrogen atom, a halogen atom, an alkyl, aryl, acyl, alkoxycarbonyl, aryloxycarbonyl, carbamoyl, nitro, cyano, alkylsulfonyl arylsulfonyl, hydroxy, alkoxy, aryloxy, acyloxy, acylthio, amido, alkanesulfonyloxy, or arenesulfonyloxy group;
  • X.sub. ⁇ represents a conjugate base of Bronsted acid except for F.sub. ⁇ , Cl.sub. ⁇ , Br.sub. ⁇ and I.sub. ⁇ which are conjugate bases of hydrogen halides; and R 1 , R 2 , R 3 , R 4 and R 5 may be combined together directly or through a hetero
  • the present invention further relates to a process for producing the above N-fluoropyridinium salt by reacting a pyridine-compound having the general formula: ##STR2## wherein R 1 to R 5 represent the same meaning as defined above, with fluorine (F 2 ) and a Bronsted acid compound having the general formula:
  • M represents a hydrogen atom, a metal atom, an ammonium residue, a pyridinium residue or a group SiR 6 R 7 R 8 in which R 6 ,R 7 and R 8 are an aklyl, aryl, alkoxy, aryloxy, acyloxy group, or a halogen atom; and X represents the same meaning as above.
  • pyridine-copmpounds set forth in formula (II) employable in the present invention are those which are easily available or which may be prepared readily and are exemplified by pyridine; straight or branched alkylated or cyclic alkylated pyridine such as methyipyridine, dimethylpyridine, trimethylpyridine, tetramethylpyridine, pentamethylpyridine, ethylpyridine, diethylpyridine, butylpyridine, dibutylpyridine, tributylpyridine, pentylpyridine, hexylpyridine, decylpyridine, (trifluoromethyl)-pyridine, bis(trifluoromethyl)pyridine tris(trifluoromethyl)-pyridine, (trichloromethyl)pyridine, (pentafluoroethyl)-pyridine, (perfluorooctyl)pyridine, (methoxymethyl)pyridine, ethyl pyridylacetate,
  • sulfonic acids or sulfuric acids such as methanesulfonic acid, butanesulfonic acid, benzensulfonic acid, toluenesulfonic acid, nitrobenzensulfonic acid, dinitrobenzensulfonic acid, trinitrobenzensulfonic acid, trifluoromethanesulfonic acid, perfluorobutanesulfonic acid, perfluorooctanesulfonic acid, trichloromethanesulfonic acid, diflurormethanesulfonic acid, trifluoroethanesulfonic acid, fluorosulfonic acid, chlorosulfonic acid, monomethylsulfric acid, sulfuric acid, camphorsulfonic acid, bromocamphorsulfonic acid, ⁇ 4 -cholest
  • .Iadd.Bronsted .Iaddend.acids a variety of ammonium salts or pryidinium salts of the above mentioned .[.Brosted.]. .Iadd.Bronsted .Iaddend.acids; silyl compounds resulting from the substitution of hydrogen atom or atoms of the above mentioned .[.Brosted.]. .Iadd.Bronsted .Iaddend.acids with a group SiR 6 R 7 R 8 wherein R 6 , R 7 and R 8 are the same as defined above, or metal bifluoride such as sodium bifluoride, for example.
  • the group SiR 6 R 7 R 8 there may be listed, for example, trimethylsilyl, triethylsilyl, dimethylbutylsilyl, dimethylphenylsilyl, triphenylsilyl, trihalosilyl, triacetylsilyl, triacetoxysilyl, trimethoxysilyl, triphenoxysilyl.
  • the metals for the metal salts of Brosted acids reference is preferably made to alkali metals or alkaline earth metals from the aspect of economy and reaction efficiency.
  • ammonium salts or pyridinium salts there may be mentioned ammonium salts, trimethylammonium salts, triethylammonium salts, tetraethylammonium salts, benzyltrimethylammonium salts, phenylammonium salts, dimethylphenylammonium salts, naphthaylammonium salts, pryidinium salts, dimethylpyridinium salts, trimethylpyridinium salts, quinolinium salts and the like.
  • the pyridinium compounds represented by formula (II) as the raw material include, for example, sodium pyridinesulfonate, pyridinesulfonic acid, ammonium pyridinesulfonate, potassium pyridylethylsulfonate, sodium pyridinecarboxylate and the like.
  • the pyridine.F 2 complex where X.sub. ⁇ represents F.sub. ⁇ which is the conjugatge base of hydrogen halide in the N-fluoropyridinium salts has a serious drawback in that it is unstable and explodes at a temperature above -2° C. and when the conjugate base is Cl.sub. ⁇ , Br.sub. ⁇ or I.sub. ⁇ the corresponding N-fluoropyridinium salts are difficult in synthesis.
  • the Brosted acid-compounds for achieving better reaction efficiencies should be equal to or in excess molar amount to that of the host material, but preferably should be an equi-molar amount from an economic viewpoint.
  • Fluorine employed in the present invention should preferably be diluted with 50 to 99.9% by volume of an inert gas in order to suppress any violent reactions.
  • the diluting gas includes, by way of example, nitrogen, helium, argon, tetrafluoromelthane, sulfur hexafluoride and the like.
  • the fluorine gas for achieving better reaction efficiencies should be used in an equi-molar or in excess molar amount to be the host material. However since the amount may vary depending upon the manner of introduction, reaction temperature, reaction solvent, reaction apparatus and so on, it may preferably be selected in amounts required for eliminating the last traces of the host material.
  • the reaction is preferably carried out by the sue of a solvent.
  • a solvent acetonitrile, methylene chloride, chloroform, carbon tetrachloride, trichlorofluoromethane, trichlorotrifluoroethane, ethyl acetate, diethyl ether, tetrahydrofuran, and the like or a mixture thereof may be used.
  • a reaction temperature of -100° to +40° C. may be selected, but the range of temperature of from -90° C. to room temperature is being preferred for better reaction yields.
  • a trapping agent such as sodium fluoride to capture hydrogen fluoride produced as a by-product.
  • N-fluoropyridinium salt having the formula (I) N-fluoropryidinium salt having the formula ##STR3## (wherein R 1 to F 5 have the same meaning as above and Y represents a Lewis acid), can be prepared by reacting the pyridine-compound represented by formula (II) with fluorine (F 2 ) and a Lewis acid having the formula
  • the Lewis acid may include, for example, boron trifluoride, boron trichloride, triacetoxyboron, tri(tgrifluoroacetoxy)boron, aluminum trifluoride, aluminum trichloride, aluminum tribromide, phosphorous trifluoride, phosphorous pentafluoride, phosphorus pentachloride, arsenic trifluoride, arsenic trichloride, arsenic pentafluoride antimony trifluoride, antimony pentafluoride, antimony dichlorotrifluoride, silicon tetrafluoride, trimethylfluorosilane, dimethylphenylfluorosilane, sulfur trioxide, titanium tetrachloride, stannic chloride, ferric chloride, and iodine pentafluoride.
  • Lewis acids may also employed without any problems.
  • These Lewis acids may be employed in an equi-molar or in excess molar amount to he host material (II) for achieving a better reaction efficiency, but from the standpoint of economy the equi-molar amount be preferable.
  • the manner in which fluroine is used and the amount of fluorine to be used are similar to the above embodiment.
  • a reaction of the present invention is preferably carried out by using a reaction solvent.
  • the reaction solvent may include, for example, acetonitrile, methylenechloride, chloroform, trichlorofluoromethane, trichlorofluoroethane, ethylacetate, diethylether, tetrahydrofuran or a mixture thereof.
  • a reaction temperature may generally be in the range of .[.-100+'° C., .]. .Iadd.-100° to +40° C. .Iaddend.and preferably a range of .[.-90+° C. .]. .Iadd.-90° to +20° C. .Iaddend.may be selected for a better yield.
  • the compounds (I) according to the present invention can be readily prepared and are in most cases stable in air at room temperature. These compounds enable the simple and selective introduction of a fluorine atom to a comtemplated compound with good efficiency and therefore serve as a superior fluorine-introducing agent. Further, the compounds according to the present invention, after they have once been reacted, reproduce the pyridine-compounds or form protonic salts of silyl salts of pyridine-compounds which can readily generate the starting pyridine-compounds by neutralization or treatment with water.
  • Example 3 was carried out as in Example 1 and Examples 4-15 were carried out as in Example 2.
  • the reactants used and the results obtained are shown in Table 1 and the physical properties of the products are shown in Table 6.
  • Examples 17-26 were carried out as in Example 16 and the results are shown in Table 2 with the physical properties in Table 6.
  • Examples 28-38 were carried out as in Example 27 except that in Examples 34 the gas ratio of fluorine:nitrogen was 2.5:97.5. The results are summarized in Table 3 with the physical properties in Table 6.
  • Example 62 to 64 were carried out as in Example 61, and the results of which are summarized in Table 5 with the physical properties in Table 6. It should be noted that the appropriate amount of boron fluoride, BF 3 , was introduced in the form of a gas, because .[.BD.]. .Iadd.BF 3 .Iaddend.is a gas, while SbF 5 and SO 3 are introduced in liquid form.
  • boron fluoride BF 3
  • a 1,1,2-trichloroethane solution (2 ml) containing 1.0 mmole of phenol and 0.5 mmole of N-fluoropyriinium trifluoromethanesulfonate was heated at 100° C. for 24 hours under an argon atmosphere and 0.25 mmole of additional N-fluoropyridinium trifluoromethanesulfonate, was added both after 3 hours and 6 hours, thus bringing the total amount of N-fluoropyridinium trifluoromethanesulfonate to 1.0 mmole.
  • the resulting reaction solution was subjected to gas chromatography to reveal that it contained 0.40 mmole of o-fluorophenol, 0.14 mmole of p-fluorophenol, 0.05 mmole of 2,4-difluorophenol and 0.21 mmole of phenol. Therefore, the yields of o-, p-fluorophenols and 2,4-difluoro-phenol were 51%, 18% and 6% respectively, corresponding to the total yields to 75%, with the total conversion of 79%.
  • fluorine-containing compounds were prepared by reacting N-fluoropyridinium salts according to the present invention with an equi-molar amount of compounds contemplated to be fluorinated. These examples were carried out similar to Example 66 with the reaction conditions set forth in Tables 7-10. The results obtained are also indicated in Tables 7-10. The identification of the structures of the resulting compounds were effected by comparing those with a standard specimem or with spectroscopy.

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Abstract

A pyridine-compound is reacted with fluorine together with a .[.Bronsted.]. .Iadd.Bronsted .Iaddend.acid-compound or Lewis acid to form a N-fluoropyridinium salt which is very active to other compounds but is very selective for the preparation of a desired product and this product is very useful for a fluorine-introducing agent which makes it useful for the preparation of fluoro-compounds such as thyroid inhibitor.

Description

.[.This application is a continuation of application Ser. No. 022,275, filed Mar. 5, 1987, now abandoned, which was a continuation-in-part application of Ser. No. 870,010, filed Jun. 3, 1986, now abandoned..]..Iadd.
CROSS REFERENCE
This application is a Re-issue of Ser. No. 07/296,411 filed Jan. 09, 1989, U.S. Pat. No. 4,996,320, which is a Continuation of Ser. No. 07/022,275 filed Mar. 05, 1987, (abandoned), which is a Continuation-in-part of Ser. No. 06/870,010 filed Jun. 03, 1986 (abandoned). .Iaddend.
BACKGROUND OF THE INVENTION
The present invention relates to a N-fluoropyridinium salt and a process for preparing same. The N-fluoropyridinium salts according to the present invention are very useful as a fluorine atom introducing agent as seen from the examples 66-133 hereinafter illustrated. The salts according to the invention have a widespread use because of their high reactivity with a wide variety of compounds and selectivity for any desired products. For example, said salt can be used for the preparation of 3-fluoro-4-hydroxyphenlacetic acid which is useful as a thyroid inhibitor by reacting the former with p-hydroxyphenylacetate followed by a common hydrolysis reaction as illustrated in examples 79 to 82 referred to hereinafter.
Heretofore, it has been well known in the art that fluorine compounds are significantly distinguished from chlorine compounds, bromine compounds, and iodine compounds in their physical properties and reactivities, because fluorine atom have characteristics such as very high electronegativity, high ionization energy, extremely high bonding ability with other atoms, small Van der Waals diameter, lack of a d-electron orbit and the like (N. Ishikawa & Y. Kobayashi; FLUORINE COMPOUNDS; THEIR CHEMISTRY AND APPLICATIONS; KodanshaSchientific, pp. 69-70. 1979). Therefore, fluorination reactions naturally have significantly different aspects from other halogenation reactions such as chlorinations, brominations and iodinations.
In reactions with organic compounds, fluorine, contrary to chlorine, bromine and iodine, reacts very violently, readily giving rise to the fission of the C--C bond of organic compounds and in cases where the reaction is excessively violent, fire or explosion in turn can break out. The abnormality of fluorination reactions relative to other halogenation reactions may be readily understood from the comparison of heat of formation in halogenation reactions (see the description on pages 69-75 of the above article) as follows:
______________________________________                                    
              ΔH (Kcal/mol)                                         
type of reaction                                                          
                X = F   Cl       Br   I                                   
______________________________________                                    
C═C + X.sub.2 --CX--CX                                                
                -111    -36      -23  -16                                 
C--H + X.sub.2 --C--X + HX                                                
                -105    -25       -9   +6                                 
______________________________________
As seen from the above Table, since the heat of reaction in the fluorination reactions amount to ever 100Kcal/-mol, while the bonding energy between carbon-carbon atoms is approximately only 60Kcal/mol, the control of fluorination reactions is very difficult, contrary to other halogenation reactions. Accordingly, the development of fluorination reactions having better selectivity has been an important subject matter in fluorination industries.
For the purpose resolving the above problem, a wide variety of compoounds for introducing fluorine atoms have heretofore been studied and developed. As such compounds, for example, trifluoromethyl-hypofluorite (CF3 OF), trifluoroacetyl-hypofluorite (CF3 COOF), acetyihypofluorite (CH3 COOF), xenon difluoride XeF2), FClO3, sulfur tetrafluoride (SF4), die-thylaminosulfur trifluoride (ET2 NSF3), CClHFCF2 NEt2,CF3 CFHCF2 NEt2, heavy metal fluorides such as AgF, HgF, CoF3,AgF2 and the like were known in the art (see pages 79-94 of the above-mentioned article). However, these compounds have drawbacks such as poor selectivity for the desired reaction, are highly hazardous to handle, have high cost, unstableness, a limited scope of application, and the like which make them commercially unsatisfactory. On the other hand, hydrogen fluoride, hydrofluoric acid, potassium fluoride, cesium fluoride, and the like which are known as inexpensive agents for introducing fluorine atoms are inferior in electrophilic reactivity, which imposes such limitations that they cannot perform electrophilic substitutions for aromatic nuclei or negatively charged carbon ions. These compounds also present serious problems in handling because hydrogen fluoride or hydrofluoric acid, for example, are highly toxic. It has been suggested that a pyridine. F2 complex can be used as a fluorine atom-introducing agent, but it can only offer low total yield of fluorination reactions [see, Z. Chem., 12, 292 (1972)] and moreover, said complex is highly hygroscopic and thermally unstable so that explosions may break out at above -2°C. [Z. Chem., 5, 64 (1965)]. From the above, it can hardly be said that the complex is a useful fluorinating agent. Recently, N-fluoro-N-alkylarenesulfoneamide have been reported as fluorine atom-introducing agents, but these compounds are low in reactivity and only effective for particular reaction species (negatively charged carbon ions) [J. Amer. Chem. Soc. 106, 452 (1984)]. Therefore, a strong need exists for the development of highly satisfactory fluorine atom-introducing agents.
As a result of a series of earnest investigations by the present inventors towards the development of a novel fluorine-introducing agent, they have succeeded in developing a novel fluorine-introducing agent which is active but stable allowing the easy handling of the agent which still retains high selectivity of a desired reaction, thus completing the present invention. The compounds according to the present invention have high reactivity with a variety of compounds and high selectivity for any desired compounds, which allows the compounds to be very useful for the synthesis of a variety of fluorine-containing compounds in a shortened process. For example, a thyroid inhibitor, 3-fluoro4-hydroxy-phenylacetic acid could easily be prepared from p-hydorxyphenylacetate available industrially (see, Examples 79-82 hereinafter described).
SUMMARY OF THE INVENTION
The present invention relates to a N-fluoropyridiuium salt represented by the formula: ##STR1## wherein R1, R2, R3, R4 and R5 represent a hydrogen atom, a halogen atom, an alkyl, aryl, acyl, alkoxycarbonyl, aryloxycarbonyl, carbamoyl, nitro, cyano, alkylsulfonyl arylsulfonyl, hydroxy, alkoxy, aryloxy, acyloxy, acylthio, amido, alkanesulfonyloxy, or arenesulfonyloxy group; X.sub.⊖ represents a conjugate base of Bronsted acid except for F.sub.⊖, Cl.sub.⊖, Br.sub.⊖ and I.sub.⊖ which are conjugate bases of hydrogen halides; and R1, R2, R3, R4 and R5 may be combined together directly or through a hetero atom or atoms in a variety of combinations to form a cyclic structure, while X.sub.⊖ may be combined directly or through a hertro-atom or atoms with R1, R2, R3, R4 and R5 in various combinations.
The present invention further relates to a process for producing the above N-fluoropyridinium salt by reacting a pyridine-compound having the general formula: ##STR2## wherein R1 to R5 represent the same meaning as defined above, with fluorine (F2) and a Bronsted acid compound having the general formula:
XM                                                         (III)
wherein M represents a hydrogen atom, a metal atom, an ammonium residue, a pyridinium residue or a group SiR6 R7 R8 in which R6,R7 and R8 are an aklyl, aryl, alkoxy, aryloxy, acyloxy group, or a halogen atom; and X represents the same meaning as above.
DETAILED DESCRIPTION OF THE INVENTION
The pyridine-copmpounds set forth in formula (II) employable in the present invention are those which are easily available or which may be prepared readily and are exemplified by pyridine; straight or branched alkylated or cyclic alkylated pyridine such as methyipyridine, dimethylpyridine, trimethylpyridine, tetramethylpyridine, pentamethylpyridine, ethylpyridine, diethylpyridine, butylpyridine, dibutylpyridine, tributylpyridine, pentylpyridine, hexylpyridine, decylpyridine, (trifluoromethyl)-pyridine, bis(trifluoromethyl)pyridine tris(trifluoromethyl)-pyridine, (trichloromethyl)pyridine, (pentafluoroethyl)-pyridine, (perfluorooctyl)pyridine, (methoxymethyl)pyridine, ethyl pyridylacetate, pyridylacetonitrile, pyridylacetone, and the like; halopyridines such as chloropyridine, bromopyridine, fluoropyridine, dichloropyridine, difluoropyridine, trichloropyridine, tetrachloropyridine, pentachloropyridine, trifluoropyridine, pentafluoropyridine, chlorofluoropyridine, dichlorofluoropyridine, and so on; (trifluoromethyl)chloropyridine, (trifluoromethyl)dichloropyridine, (trifluoromethyl)trichloropyridine, (trifluoromethyl)fluoropyridine, methylchloropyridine, phenylpyridine, diphenylpyridine, triphenylpyridine,-dipyridyl, acetylpyridine, bisacetylpyridine, benzoylpyridine;(alkoxycarbonyl)pyridine or (aryloxycarbonyl)pyridine such as (methoxycarbonyl)-pyridine,(exthoxycarbonyl)pyridine,(butoxycarbonyl)pyridine, bis(ethoyxcarbonyl)pyridine,bis(trifluoroethoxycarbonyl)-pyridine, tris(methoxycarbonyl)pyridine,(-phenoxycarbonyl)-pryidine; 2,3-pryidinedicarboxylic anhydride,nitropyridine, cyanopyridine, dicyanopyridine, tricyanopyridine, benzenesulfonylpyridine, methylsulfonylpyridine, chlorocyanopyridine, formylpyridine, (haloformyl)pyridine, nicotinamide,picolinamide, (dimethylaminocarbonyl)pyridine, methoxypyridine, dimethoxypyridine, propoxypyridine, butoxypyridine, menthoxypyridine, trifluoromethoxypyridine, acetoxypridine, trifluoroacetoxypyridine, phenoxypyridine, acetylthipoyridine, methanesulfonyloxypyridine, benzenesulfonyloxypyridine, acetylaminopyridine,3-hydroxypyridine, and 1,2,3,4,5,6,7,8-octahydroacridine.
As the .[.Brosted.]. .Iadd.Bronsted .Iaddend.acid-compounds represented by the formula (III), there may be mentioned the following compounds: sulfonic acids or sulfuric acids such as methanesulfonic acid, butanesulfonic acid, benzensulfonic acid, toluenesulfonic acid, nitrobenzensulfonic acid, dinitrobenzensulfonic acid, trinitrobenzensulfonic acid, trifluoromethanesulfonic acid, perfluorobutanesulfonic acid, perfluorooctanesulfonic acid, trichloromethanesulfonic acid, diflurormethanesulfonic acid, trifluoroethanesulfonic acid, fluorosulfonic acid, chlorosulfonic acid, monomethylsulfric acid, sulfuric acid, camphorsulfonic acid, bromocamphorsulfonic acid, Δ4 -cholestene-3-on-6-sulfonic acid, 1-hydroxy- p-methane-2-sulfonic acid, p-styrenesulfonic acid, β-styrenesulfonic acid, poly(p-styrenesulfonic acid), vinyl-sulfonic poly(vinylsulfonic acid), poly(2-acrylamide-2-methyl-1-propanesulfonic acid), and a copolymer of said propanesulfonic acid with styrene, perfluoro-3,5-dioxa-4-methyl-7-octenesulfonic acid, poly(-perfluoro-3,6-dioxa-4-methyl-7-octensulfonic acid) and a copolymer of said octnesulfonic acid with tetrafluoroethylene, and the like; phosphoric acid; nitric acid; halogen acids such as perchloric acid, perbromic acid, periodic acid, chloric acid, bromic acid, and the like; carboxylic acids such as acetic acid, formic acid, trichloro-acetic acid, trifluoroacetic acid, pentafluoropropionic acid, dichloroacetic acid, acrylic acid, poly(acrylic acid), poly-(perfluoro-3,6-dioxa-4-methyl-7-octenoic acid) and a copolymer of said octenoic acid with tetrafluoroethylene and so on; compounds resulting from hydrogen halide and Lewis acids such as HBF4, HPF6, HSbF4, HSbF6, HAsF6, HBCl3 F, HSiF5 and the like; metal salts of the above mentioned .[.Brosted.]. .Iadd.Bronsted .Iaddend.acids; a variety of ammonium salts or pryidinium salts of the above mentioned .[.Brosted.]. .Iadd.Bronsted .Iaddend.acids; silyl compounds resulting from the substitution of hydrogen atom or atoms of the above mentioned .[.Brosted.]. .Iadd.Bronsted .Iaddend.acids with a group SiR6 R7 R8 wherein R6, R7 and R8 are the same as defined above, or metal bifluoride such as sodium bifluoride, for example. As the group SiR6 R7 R8, there may be listed, for example, trimethylsilyl, triethylsilyl, dimethylbutylsilyl, dimethylphenylsilyl, triphenylsilyl, trihalosilyl, triacetylsilyl, triacetoxysilyl, trimethoxysilyl, triphenoxysilyl. As the metals for the metal salts of Brosted acids reference is preferably made to alkali metals or alkaline earth metals from the aspect of economy and reaction efficiency. Further, as the variety of ammonium salts or pyridinium salts, there may be mentioned ammonium salts, trimethylammonium salts, triethylammonium salts, tetraethylammonium salts, benzyltrimethylammonium salts, phenylammonium salts, dimethylphenylammonium salts, naphthaylammonium salts, pryidinium salts, dimethylpyridinium salts, trimethylpyridinium salts, quinolinium salts and the like.
Of the N-fluoropyridinium salts represented by formula (I), in the case where X.sub.⊖ and R1, R2, R3, R4 and R5 are combined together in a variety combinations, the pyridinium compounds represented by formula (II) as the raw material include, for example, sodium pyridinesulfonate, pyridinesulfonic acid, ammonium pyridinesulfonate, potassium pyridylethylsulfonate, sodium pyridinecarboxylate and the like.
The pyridine.F2 complex where X.sub.⊖ represents F.sub.⊖ which is the conjugatge base of hydrogen halide in the N-fluoropyridinium salts has a serious drawback in that it is unstable and explodes at a temperature above -2° C. and when the conjugate base is Cl.sub.⊖, Br.sub.⊖ or I.sub.⊖ the corresponding N-fluoropyridinium salts are difficult in synthesis.
The Brosted acid-compounds for achieving better reaction efficiencies should be equal to or in excess molar amount to that of the host material, but preferably should be an equi-molar amount from an economic viewpoint. Fluorine employed in the present invention should preferably be diluted with 50 to 99.9% by volume of an inert gas in order to suppress any violent reactions. The diluting gas includes, by way of example, nitrogen, helium, argon, tetrafluoromelthane, sulfur hexafluoride and the like.
The fluorine gas for achieving better reaction efficiencies should be used in an equi-molar or in excess molar amount to be the host material. However since the amount may vary depending upon the manner of introduction, reaction temperature, reaction solvent, reaction apparatus and so on, it may preferably be selected in amounts required for eliminating the last traces of the host material.
The reaction is preferably carried out by the sue of a solvent. As the solvent, acetonitrile, methylene chloride, chloroform, carbon tetrachloride, trichlorofluoromethane, trichlorotrifluoroethane, ethyl acetate, diethyl ether, tetrahydrofuran, and the like or a mixture thereof may be used.
A reaction temperature of -100° to +40° C. may be selected, but the range of temperature of from -90° C. to room temperature is being preferred for better reaction yields.
In carrying out the process of the present invention it is occasionally preferable for improving the reaction efficiency to employ a trapping agent such as sodium fluoride to capture hydrogen fluoride produced as a by-product.
Of the N-fluoropyridinium salts having the formula (I), N-fluoropryidinium salt having the formula ##STR3## (wherein R1 to F5 have the same meaning as above and Y represents a Lewis acid), can be prepared by reacting the pyridine-compound represented by formula (II) with fluorine (F2) and a Lewis acid having the formula
Y                                                          (IV)
The Lewis acid, the starting material set forth in formula (IV), may include, for example, boron trifluoride, boron trichloride, triacetoxyboron, tri(tgrifluoroacetoxy)boron, aluminum trifluoride, aluminum trichloride, aluminum tribromide, phosphorous trifluoride, phosphorous pentafluoride, phosphorus pentachloride, arsenic trifluoride, arsenic trichloride, arsenic pentafluoride antimony trifluoride, antimony pentafluoride, antimony dichlorotrifluoride, silicon tetrafluoride, trimethylfluorosilane, dimethylphenylfluorosilane, sulfur trioxide, titanium tetrachloride, stannic chloride, ferric chloride, and iodine pentafluoride. Ethereal complexes of these Lewis acids may also employed without any problems. These Lewis acids may be employed in an equi-molar or in excess molar amount to he host material (II) for achieving a better reaction efficiency, but from the standpoint of economy the equi-molar amount be preferable. The manner in which fluroine is used and the amount of fluorine to be used are similar to the above embodiment.
A reaction of the present invention is preferably carried out by using a reaction solvent. The reaction solvent may include, for example, acetonitrile, methylenechloride, chloroform, trichlorofluoromethane, trichlorofluoroethane, ethylacetate, diethylether, tetrahydrofuran or a mixture thereof.
A reaction temperature may generally be in the range of .[.-100+'° C., .]. .Iadd.-100° to +40° C. .Iaddend.and preferably a range of .[.-90+° C. .]. .Iadd.-90° to +20° C. .Iaddend.may be selected for a better yield.
The compounds (I) according to the present invention can be readily prepared and are in most cases stable in air at room temperature. These compounds enable the simple and selective introduction of a fluorine atom to a comtemplated compound with good efficiency and therefore serve as a superior fluorine-introducing agent. Further, the compounds according to the present invention, after they have once been reacted, reproduce the pyridine-compounds or form protonic salts of silyl salts of pyridine-compounds which can readily generate the starting pyridine-compounds by neutralization or treatment with water.
The following examples will illustrate the present invention in more detail.
EXAMPLE 1 Preparation of N-fluoropyridiniumtrifluoromethanesulfonate ##STR4##
To a 50 ml trichlorofluoromethane solution containing 1.0 g (12.6 m moles) of pyridine a mixed gas of fluorine and nitrogen in a volumetric ratio of 1:9 was introduced at a rate of 30 ml/min. at -78° C. under vigorous stirring. The amount of the fluorine gas introduced amounted to 34.8 mmoles. Subsequent to the fluorine introduction, 20 ml of anhydrous acetonitrile and 2.2 g (12.8 mmoles) of sodium trifluoro-methanesulfonate as a XM reactant were added to the reaction solution after which the temperature of the solution was raised to -40° C., while removing the solvent with the aid of an aspirator. The solvent, after filtering sodium fluoride formed as a byproduct, was distilled off and the resultant residue was recrystallized from THF to give 1.75 g (yield: 67%) of N-fluoropyridinium trifluoromethanesulfonate, the physical properties of which are shown in Table 6.
EXAMPLE 2 Preparation of N-fluoropyridiniumtrifluoromethanesulfonate ##STR5##
To a 100 ml anhydrous acetonitrile solution containing 10 g (0.126 mole) of pyridine a mixed gas of fluorine and nitrogen was introduced at a rate of 90 ml/min. at -4020 C. under virorous stirring. The amount of the flourine gas introduced amounted to 0.18 mole. Subsequent to the fluorine introduction, 22 g (0.128 mole) of sodium trifluoromethanesulfonate as a XM reactant was added to the reaction solution after which the resultant reaction solution was maintained at -40° C. for 5 hours under stirring. Subsequently, the solvent, after filtering sodium fluoride, was distilled off and the resultant residue was recrystallized from methylene chloride to give 17.5 g (yield: 71%) of N-fluoropyridinium trifluoromethanesulfonate. The product thus obtained was repurified with methylene chloride/acetonitrile to recover 13.8 g (yield: 56%).
EXAMPLES 3-15
Example 3 was carried out as in Example 1 and Examples 4-15 were carried out as in Example 2. The reactants used and the results obtained are shown in Table 1 and the physical properties of the products are shown in Table 6.
Further, Example 12 employed sodium D-camphorsulfonate as the XM reactant and the angle of specific rotatory power of the product was [α]D 22 =+29.51 (c=0.664, CH3 CN).
                                  TABLE 1                                 
__________________________________________________________________________
     pyridine-                                             yield          
Example                                                                   
     compound        XM            product                 (%)            
__________________________________________________________________________
      ##STR6##       CF.sub.3 SO.sub.3 Na                                 
                                    ##STR7##               60             
4                                                                         
      ##STR8##       NaPF.sub.6                                           
                                    ##STR9##               34             
5                                                                         
      ##STR10##      NaSbF.sub.6                                          
                                    ##STR11##              51             
6                                                                         
      ##STR12##      NaClO.sub.4                                          
                                    ##STR13##              72             
7                                                                         
      ##STR14##      CF.sub.3 SO.sub.3 H                                  
                                    ##STR15##              44             
8                                                                         
      ##STR16##      CF.sub.3 SO.sub.3 SiMe.sub.3                         
                                    ##STR17##              45             
9                                                                         
      ##STR18##      CF.sub.3 SO.sub.3 H                                  
                                    ##STR19##              41             
10                                                                        
      ##STR20##      CF.sub.3 SO.sub.3 SiMe.sub.3                         
                                    ##STR21##              62             
11                                                                        
      ##STR22##      FSO.sub.3 H                                          
                                    ##STR23##              49             
12                                                                        
      ##STR24##                                                           
                      ##STR25##                                           
                                    ##STR26##              50             
13                                                                        
      ##STR27##      FSO.sub.3 H                                          
                                    ##STR28##              56             
14                                                                        
      ##STR29##      CF.sub.3 COOSiMe.sub.3                               
                                    ##STR30##              77             
15                                                                        
      ##STR31##      CF.sub.3 SO.sub.3 H                                  
                                    ##STR32##              60             
__________________________________________________________________________
EXAMPLE 16 ##STR33##
In 20 ml of anhydrous acetonitrile 0.50 g (4.67 mmoles) of 2.6- dimethylpyridine and 0.803 g (4.67 mmoles) of sodium trifluoromethanesulfonate as the XM reactant were dissolved, and to the resultant solution a mixed gas of fluorine and nitrogen (1:9) was added at a rate of 30 ml/min. at -40° C. under vigorous stirring. The amount of the fluorine gas introduced amounted to 8.93 mmoles. After the completion of the reaction, sodium fluoride was filtered and the solvent was distilled off. The resultant residue was recrystallized from THF to give 0.88 g (yield: 73%) of N-fluoro-2,6-diemthyl-pyridinium trifluoromethanesulfonate. The resultant product was further recrystallized with THF/acetonitrile to obtain 0.82 g (yield: 69%), the physical properties of which are shown in Table 6.
EXAMPLES 17-26
Examples 17-26 were carried out as in Example 16 and the results are shown in Table 2 with the physical properties in Table 6. In Example 22, 2 -1-menthoxypyridine [[α]D20 =-110.7 (c=0.994, CHCl3)] was used as the pyridine compound for the starting material and the specific rotary power of the resultant N-fluoro-2-1-menthoxypyridinium trifluoromethanesulfonate was [α]D25 =-77.73 (c=4.16, CHCl3).
                                  TABLE 2                                 
__________________________________________________________________________
     Pyridine-                                 Yield                      
Example                                                                   
     Compound         XM     Product           (%)                        
__________________________________________________________________________
17                                                                        
      ##STR34##       CF.sub.3 SO.sub.3 Na                                
                              ##STR35##        82                         
18                                                                        
      ##STR36##       CF.sub.3 SO.sub.3 Na                                
                              ##STR37##        72                         
19                                                                        
      ##STR38##       n-C.sub.4 F.sub.9 SO.sub.3 Na                       
                              ##STR39##        87                         
20                                                                        
      ##STR40##       CF.sub. 3 SO.sub.3 Na                               
                              ##STR41##        60                         
21                                                                        
      ##STR42##       CF.sub.3 SO.sub.3 Na                                
                              ##STR43##        73                         
22                                                                        
      ##STR44##       CF.sub.3 SO.sub.3 Na                                
                              ##STR45##        57                         
23                                                                        
      ##STR46##       CF.sub.3 SO.sub.3 Na                                
                              ##STR47##        90                         
24                                                                        
      ##STR48##       CF.sub.3 SO.sub.3 Na                                
                              ##STR49##        19                         
25                                                                        
      ##STR50##       CF.sub.3 SO.sub.3 H                                 
                              ##STR51##        75                         
26                                                                        
      ##STR52##       CF.sub.3 SO.sub.3 Na                                
                              ##STR53##        60                         
Example 27                                                                
 ##STR54##
To a 5 ml anhydrous acetonitrile solution containing 0.408 g (5.17 mmoles) of pyridine, 1.0 ml (5.17 mmoles) of trimethylsilyl trifluoromethanesulfonate as the XM reactant was added at -40° C. under stirring. To the resultant solution a mixed gas of fluorine and nitrogen (1:9), 10 minutes after the addition, was introduced at a rate of 15 ml/min. The amount of fluorine gas introduced was 15.5 mmoles. After the completion of the reaction, an amount of ether cooled to -60° C. was added to the solution to precipitate crystals which were filtered to give 0.99 g (yield: 78%) of N-fluoropyridinium trifluoromethanesulfonate.
EXAMPLES 28-38
Examples 28-38 were carried out as in Example 27 except that in Examples 34 the gas ratio of fluorine:nitrogen was 2.5:97.5. The results are summarized in Table 3 with the physical properties in Table 6.
                                  TABLE 3                                 
__________________________________________________________________________
     Pyridine-                                  Yield                     
Example                                                                   
     Compound         XM       Product          (%)                       
__________________________________________________________________________
28                                                                        
      ##STR55##       CH.sub.3 SO.sub.3 SiMe.sub.3                        
                                ##STR56##       42                        
29                                                                        
      ##STR57##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                                ##STR58##       55                        
30                                                                        
      ##STR59##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                                ##STR60##       79                        
31                                                                        
      ##STR61##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                                ##STR62##       71                        
32                                                                        
      ##STR63##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                                ##STR64##       69                        
33                                                                        
      ##STR65##       CF.sub.3 SO.sub.3 SiMe.sub.2 Ph                     
                                ##STR66##       71                        
34                                                                        
      ##STR67##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                                ##STR68##       68                        
35                                                                        
      ##STR69##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                                ##STR70##        30                       
36                                                                        
      ##STR71##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                                ##STR72##       28                        
37                                                                        
      ##STR73##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                                ##STR74##       52                        
38                                                                        
      ##STR75##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                                ##STR76##       86                        
__________________________________________________________________________
.Iadd.EXAMPLE 39 .Iaddend. ##STR77##
In a 25 ml pear-shaped flask, 2,4,6-trimethylpyridine (1.21 g, 10 mmoles), sodium borofluoride (1.23 g 10 mmoles) as the XM reactant and anhydrous sodium fluoride (2.1 g, 50 mmoles) were dissolved in 15 ml of anhydrous acetonitrile and to the resulting solution a mixed gas of nitrogen/fluorine (9:1) was introduced at a rate of 50 ml/min. at -40 ° C. under vigorous stirring.
The amount of fluorine introduced was 20 mmoles. After the completion of the reaction, precipitates were filtered and then the solvent was distilled off. The resultant residue was recrystallized from acetonitrile/diethylether to obtain 1.59 g (yield: 70%)of N-fluoro-2,4,6-trimethylpyridinium tetrafluoroborate the physical properties of which are shown in Table 6.
EXAMPLE 40 ##STR78##
This example was effected as in example 39 to give N-fluoro-4-methylpyridinium trifluoromethanesulfonate in 90% yield, the physical properties of which are indicated in Table 6.
EXAMPLE 41-60
Further examples were carried out by using various pyridine compounds and XM. The experimental methods, the reaction products and the yeilds are shown in Table 4. The physical properties of the products are indicated in Table 6.
                                  TABLE 4                                 
__________________________________________________________________________
Ex-                                Ex-                                    
am- Pyridine                  Trapping                                    
                                   perimental              Yield          
ple Compound          XM      Agent                                       
                                   Method                                 
                                         Product           (%)            
__________________________________________________________________________
41                                                                        
     ##STR79##        CF.sub.3 SO.sub.3 Na                                
                              --   Ex. 16                                 
                                          ##STR80##        76             
42                                                                        
     ##STR81##        CF.sub.3 SO.sub.3 Na                                
                              NaF  Ex. 39                                 
                                          ##STR82##        86             
43                                                                        
     ##STR83##        NaBF.sub.4                                          
                              NaF  Ex. 39                                 
                                          ##STR84##        65             
44                                                                        
     ##STR85##        CF.sub.3 SO.sub.3 Na                                
                              NaF  Ex. 39                                 
                                          ##STR86##        26             
45                                                                        
     ##STR87##        NaClO.sub.4                                         
                              --   Ex. 39                                 
                                          ##STR88##        81             
46                                                                        
     ##STR89##        CF.sub.3 SO.sub.3 SiMe.sub.3                        
                              --   Ex. 27                                 
                                          ##STR90##        60             
47                                                                        
     ##STR91##        CF.sub.3 SO.sub.3 Na                                
                              NaF  Ex. 39                                 
                                          ##STR92##        87             
48                                                                        
     ##STR93##        CF.sub.3 SO.sub.3 Na                                
                              NaF  Ex. 39                                 
                                          ##STR94##        62             
49                                                                        
     ##STR95##        CF.sub.3 SO.sub.3 Na                                
                              --   Ex. 16                                 
                                          ##STR96##        72             
50                                                                        
     ##STR97##        CF.sub.3 SO.sub.3 Na                                
                              NaF  Ex. 39                                 
                                          ##STR98##         33            
51                                                                        
     ##STR99##        CF.sub.3 SO.sub.3 SiMe.sub.3                        
                              NaF  Ex. 39                                 
                                          ##STR100##       18             
52                                                                        
     ##STR101##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                              --   Ex. 2                                  
                                          ##STR102##       15             
53                                                                        
     ##STR103##       CF.sub.3 SO.sub.3 Na                                
                              NaF  Ex. 39                                 
                                          ##STR104##       1.3            
54                                                                        
     ##STR105##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                              --   Ex. 1                                  
                                          ##STR106##       little         
55                                                                        
     ##STR107##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                              --   Ex. 1                                  
                                          ##STR108##       little         
56                                                                        
     ##STR109##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                              --   Ex. 27                                 
                                          ##STR110##       68             
57                                                                        
     ##STR111##       CF.sub.3 SO.sub.3 Na                                
                              NaF  Ex. 39                                 
                                          ##STR112##       84             
58                                                                        
     ##STR113##       CF.sub.3 SO.sub.3 Na                                
                              NaF  Ex. 39                                 
                                          ##STR114##       56             
 59*                                                                      
     ##STR115##       CF.sub.3 SO.sub.3 Na                                
                              Na.sub.2 CO.sub.3                           
                                   Ex. 39                                 
                                          ##STR116##       10             
60                                                                        
     ##STR117##       CF.sub.3 SO.sub.3 SiMe.sub.3                        
                              --   Ex. 1                                  
                                          ##STR118##       little         
__________________________________________________________________________
 *Acetonitrile-water (1:1) is used as a reaction medium.
EXAMPLE 61 ##STR119##
To a 30 ml anhydrous acetonitrile solution containing 0.71 g (8.98 mmole) of pyridine a mixed gas of fluorine and nitrogen (1:9) was introduced at a rate of 20 ml/min. at -40° C. under vigorous stirring, the amount of fluorine gas introduced being 26 mmoles. Subsequently, at the same temperature, 1 ml (8.13 mmole) of an ethereal complex of boron trifluoride as the Lewis acid was added and the resulting solution was stirred for 5 hours. The post treatment was effected as in example 13 to give 0.91 g (yield: 69%) of N-fluoropyridinium tetrafluoroborate, the physical properties of which are reproduced in Table 6.
EXAMPLES 62-64
These Examples 62 to 64 were carried out as in Example 61, and the results of which are summarized in Table 5 with the physical properties in Table 6. It should be noted that the appropriate amount of boron fluoride, BF3, was introduced in the form of a gas, because .[.BD.]. .Iadd.BF3 .Iaddend.is a gas, while SbF5 and SO3 are introduced in liquid form.
                                  TABLE 5                                 
__________________________________________________________________________
Example                                                                   
     Pyridine-   Lewis             Yield                                  
No.  Compound    Acid                                                     
                     Product       (%)                                    
__________________________________________________________________________
62                                                                        
      ##STR120## BF.sub.3                                                 
                      ##STR121##   62                                     
63                                                                        
      ##STR122## SbF.sub.5                                                
                      ##STR123##   37                                     
64                                                                        
      ##STR124## SO.sub.3                                                 
                      ##STR125##   46                                     
Example 65                                                                
 ##STR126##                                                               
This Example was carried out as in Example 16 except that boron           
trifluoride etherate was used in place of sodium trifluoromethanesulfonate
 to obtain N-fluoro- 3,5-dichloropyridinium tetrafluoroborate (yield:     
79%), the physical properties of which are given in Table 6.              

TABLE 6                                                                   
__________________________________________________________________________
Physical Properties of N-fluoropyridinium Salts                           
                                           Elemental analysis             
                 F-NMR (ppm)               (Calculated)                   
Example No.                                                               
       Melting Point (°C.)                                         
                 (CFCl.sub.3 internal standard in CD.sub.3 CN)            
                                   Mass (m/e)                             
                                           C % H % N %                    
__________________________________________________________________________
1, 2, 7, 8, 27                                                            
       185-187   -48.75 (1F, bs, NF)                                      
                                   227(M.sup.+ -HF)                       
                                           29.17                          
                                               1.99                       
                                                   5.66                   
                 77.61 (3F, s, CF.sub.3)   (29.16)                        
                                               (2.04)                     
                                                   (5.67)                 
3      41-42     -46.89 (1F, bs, NF)                                      
                                   255(M.sup.+ -H)                        
                                           34.72                          
                                               3.35                       
                                                   5.07                   
                 77.75 (3F, s, CF.sub.3)   (34.91)                        
                                               (3.30)                     
                                                   (5.09)                 
4       202      -48.58 (1F, bs, NF)                                      
                                   174, 172                               
                                           24.84                          
                                               2.10                       
                                                   5.65                   
       (decomposition)                                                    
                 71.68 (6F, d, J = 715 Hz, PF.sub.6)                      
                                   107, 97 (24.69)                        
                                               (2.06)                     
                                                   (5.76)                 
5, 63  >300      -48.82 (1F, bs, NF)                                      
                                   278, 276                               
                                           18.02                          
                                               1.50                       
                                                   4.09                   
                 69.0-175.0 (6F, m, SbF.sub.6)                            
                                   (M.sup.+ -3F)                          
                                           (17.96)                        
                                               (1.50)                     
                                                   (4.19)                 
6        225-227.5                                                        
                 -48.75 (1F, bs, NF)                                      
                                   156, 155, 97,                          
                                           30.50                          
                                               2.23                       
                                                   7.12                   
       (with decompo.)             79      (30.38)                        
                                               (2.53)                     
                                                   (7.09)                 
9, 10, 29                                                                 
       99.5-110  -52.13 (1F, bs, NF)                                      
                                   299. 297                               
                                           22.68                          
                                               0.94                       
                                                   4.58                   
                 77.63 (3F, s, CF.sub.3)                                  
                                   295 (M.sup.+ -HF)                      
                                           (22.80)                        
                                               (0.96)                     
                                                   (4.43)                 
11     120-125   -48.18 (1F, bs, NF)                                      
                                   177 (M.sup.+ -HF)                      
                                           30.56                          
                                               2.57                       
                                                   7.03                   
                 -38.21 (1F, s, S) 149     (30.46)                        
                                               (2.56)                     
                                                   (7.10)                 
12       135-136.5                                                        
                 -17.25 (bs, NF)   151, 139                               
                                           58.00                          
                                               7.05                       
                                                   3.74                   
                                           (58.20)                        
                                               (7.05)                     
                                                   (3.77)                 
13, 64 162-164   -38.25 (1F, s, SO.sub.2 F)                               
                                   237     39.36                          
                                               4.52                       
                                                   5.90                   
       (decomposition)                                                    
                 -17.25 (1F, bs, NF)                                      
                                   219(M.sup.+ -HF)                       
                                           (40.16)                        
                                               (4.60)                     
                                                   (5.89)                 
14       24-25.5 -17.63 (1F, bs, NF)                                      
                                   --      --  --  --                     
                 75.00 (3F, s, CF.sub.3)                                  
                                   --      --  --  --                     
15, 17 168.5-170 -17.25 (1F, bs, NF)                                      
                                   139     37.15                          
                                               3.87                       
                                                   4.66                   
                 77.62 (3F, s, CF.sub.3)                                  
                                   121     (37.37)                        
                                               (3.84)                     
                                                   (4.84)                 
16     126-128   -24.75 (1F, bs, NF)                                      
                                   255(M.sup.+ -HF)                       
                                           34.86                          
                                               3.26                       
                                                   5.03                   
                 77.75 (3F, s, CF.sub.3)   (34.91)                        
                                               (3.30)                     
                                                   (5.09)                 
18, 25, 34                                                                
       140-143   -25.50 (1F, bs, NF)                                      
                                   227, 137, 69,                          
                                           30.31                          
                                               2.52                       
                                                   5.07                   
                 77.61 (3F, s, CF.sub.3)                                  
                                   59      (30.32)                        
                                               (2.53)                     
                                                   (5.05)                 
19     111-112   -48.37 (1F, bs, NF),                                     
                                   377(M.sup.+ -HF)                       
                                           27.08                          
                                               1.35                       
                                                   3.55                   
                 80.30 (3F, tt, J = 10.1, 3.0 Hz, CF.sub.3)               
                                           (27.22)                        
                                               (1.27)                     
                                                   (3.53)                 
                 114.2 (2F, m, CF.sub.2),                                 
                 120.9 (2F, m, CF.sub.2),                                 
                 125.2 (2F, M, CF.sub.2 S)                                
20     119.5-120.5                                                        
                 -37.13 (1F, bs, NF)                                      
                                   --      --  --  --                     
                 77.25 (3F, s, CF.sub.3)                                  
                                   --      --  --  --                     
21     95-96     -0.75 (1F, bs, NF)                                       
                                   182, 179, 128                          
                                           30.31                          
                                               2.52                       
                                                   5.07                   
                 77.58 (3F, s, CF.sub.3)                                  
                                   113, 95, 69                            
                                           (30.32)                        
                                               (2.53)                     
                                                   (5.05)                 
22       111-111.5                                                        
                 -0.75 (1F, bs, NF)                                       
                                   --      47.70                          
                                               5.87                       
                                                   3.46                   
       (decomposition)                                                    
                 77.62 (3F, s, CF.sub.3)                                  
                                   --      (47.87)                        
                                               (5.77)                     
                                                   (3.49)                 
23     111.5-112.5                                                        
                 -51.00 (1F, bs, NF)                                      
                                   243, 187, 186                          
                                           31.72                          
                                               2.02                       
                                                   4.43                   
                 77.61 (3F, s, CF.sub.3)                                  
                                   137, 135, 113                          
                                           (31.48)                        
                                               (2.30)                     
                                                   (4.60)                 
24     88- 91    -39.38 (1F, bs, NF)                                      
                                   --      --  --  --                     
                 77.63 (3F, s, CF.sub.3)                                  
                                   --      --  --  --                     
26     79-80     -25.05 (1F, bs, NF)                                      
                                   163     --  --  --                     
                 77.98 (3F, s, CF.sub.3)                                  
                                   137     --  --  --                     
28     55-58     -48.75 (1F, bs, NF) (*)                                  
                                   173 (M.sup.+ -HF)                      
                                           --  --  --                     
30     108-109   -50.59 (1F, bs, NF)                                      
                                   263, 261                               
                                           26.38                          
                                               1.53                       
                                                   5.81                   
                 70.70 (3F, s, CF.sub.3)                                  
                                   (M.sup.+ -HF)                          
                                           (26.52)                        
                                               (1.47)                     
                                                   (5.17)                 
31, 33 105-108   -54.22 (1F, bs, NF)                                      
                                   341, 199                               
                                           23.81                          
                                               1.12                       
                                                   3.98                   
                 61.50 (3F, s, CF.sub.3)                                  
                                   197     (24.05)                        
                                               (0.86)                     
                                                   (4.01)                 
                 78.10 (3F, s, CF.sub.3 S)                                
32     115-116   -50.02 (1F, bs, NF)                                      
                                   299 (M.sup.+ -HF)                      
                                           33.74                          
                                               2.73                       
                                                   4.28                   
                 77.68 (3F, s, CF.sub.3)   (33.86)                        
                                               (2.85)                     
                                                   (4.39)                 
35     57-65     -53.25 (1F, bs, NF)                                      
                                   --      --  --  --                     
                 77.61 (3F, s, CF.sub.3)                                  
                                   --      --  --  --                     
36     110-115   -36.38 (1F, bs, NF)                                      
                                   --      --  --  --                     
       (decomposition)                                                    
                 77.61 (3F, s, CF.sub.3)                                  
                                   --      --  --  --                     
37     112-116   -54.75 (1F, bs, NF)                                      
                                   --      --  --  --                     
                 77.61 (3F, s, CF.sub.3)                                  
                                   --      --  --  --                     
38     115-116   -38.44 (1F, bs, NF)                                      
                                   137, 107, 79,                          
                                           31.49                          
                                               2.28                       
                                                   4.59                   
                 78.04 (3F, s, CF.sub.3)                                  
                                   78      (31.48)                        
                                               (2.30)                     
                                                   (4.59)                 
39     215-217   -17.25 (1F, bs, NF)                                      
                                   157, 139                               
                                           42.37                          
                                               4.75                       
                                                   6.24                   
                 149.6 (4F, s, BF.sub.4)   (42.33)                        
                                               (4.88)                     
                                                   (6.17)                 
40     84-88     -40.50 (1F, bs, NF)                                      
                                   241 (M.sup.+ -HF)                      
                                           32.12                          
                                               2.87                       
                                                   5.25                   
                 77.48 (3F, s, CF.sub.3)   (32.19)                        
                                               (2.70)                     
                                                   (5.36)                 
41     149.5-152 -19.75 (1F, bs, NF)                                      
                                   --      --  --  --                     
                 78.00 (3F, s, CF.sub.3)                                  
                                   --      --  --  --                     
42     116-118   -40.05 (1F, bs, NF)                                      
                                   268 (M.sup.+ -HF)                      
                                           39.29                          
                                               4.22                       
                                                   4.50                   
                 78.02 (3F, s, CF.sub.3)                                  
                                   135, 120                               
                                           (39.60)                        
                                               (4.32)                     
                                                   (4.62)                 
43     143-145   -39.99 (1F, bs, NF)                                      
                                   138, 110                               
                                           44.21                          
                                               5.32                       
                                                   5.64                   
                 150.6 (4F, s, BF.sub.4)   (44.85)                        
                                               (5.44)                     
                                                   (5.81)                 
44     112-114   -23.63 (1F, bs, NF)                                      
                                   210, 190                               
                                           46.56                          
                                               5.89                       
                                                   3.86                   
                 78.00 (3F, s, CF.sub.3)   (46.80)                        
                                               (5.85)                     
                                                   (3.90)                 
45     146-148   -40.00 (bs, NF)   120     --  --  --                     
46     144-147   -51.88 (1F, bs, NF)                                      
                                   343 (M.sup.+ -HF),                     
                                           32.84                          
                                               2.46                       
                                                   3.84                   
                 78.00 (3F, s, CF.sub.3)                                  
                                   248, 182                               
                                           (33.07)                        
                                               (2.50)                     
                                                   (3.86)                 
47     32        -27.38 (1F, bs, NF)                                      
                                   258     30.35                          
                                               2.61                       
                                                   5.02                   
                 77.25 (3F, s, CF.sub.3)                                  
                                   257(M.sup.+ -HF),                      
                                           (30.33)                        
                                               (2.55)                     
                                                   (5.05)                 
                                   69                                     
48     viscous   -50.10 (1F, bs, NF)                                      
                                   108     --  --  --                     
                 77.20 (1F, s, CF.sub.3)                                  
49     151-152   -37.5 (1F, bs, NF)                                       
                                   --      --  --  --                     
                 77.30 (3F, s, CF.sub.3)                                  
50     136-138   -28.88 (1F, bs, NF)                                      
                                   283 (M.sup.+ -HF)                      
                                           39.84                          
                                               4.36                       
                                                   4.41                   
                 78.00 (3F, s, CF.sub.3 )                                 
                                   135     (39.60)                        
                                               (4.29)                     
                                                   (4.62)                 
51       97-97.5 -27.00 (1F, bs, NF)                                      
                                   168, 167                               
                                           51.83                          
                                               6.95                       
                                                   3.33                   
                 77.62 (3F, s, CF.sub.3)                                  
                                   149     (52.05)                        
                                               (6.99)                     
                                                   (3.37)                 
52     131-133   -19.50 (1F, bs, NF)                                      
                                   249     53.72                          
                                               3.19                       
                                                   3.42                   
                 77.25 (3F, s, CF.sub.3)                                  
                                   231     (54.10)                        
                                               (3.26)                     
                                                   (3.51)                 
53     238-239   -17.25 (1F, bs, NF)                                      
                                   266, 246                               
                                           41.20                          
                                               4.75                       
                                                   4.33                   
                 77.25 (3F, s, CF.sub.3)                                  
                                   232, 205                               
                                           (41.38)                        
                                               (4.70)                     
                                                   (4.39)                 
54     162.5-163.5                                                        
                 -15.75 (1F, bs, NF)                                      
                                   139     35.07                          
                                               3.26                       
                                                   4.43                   
                 77.72 (3F, s, CF.sub.3)                                  
                                   121     (35.18)                        
                                               (3.26)                     
                                                   (4.56)                 
                 226.5 (1F, dt, J = 45, 10.5 Hz,                          
                 CH.sub.2 F)                                              
55     160-163   -14.63 (1F, bs, NF)                                      
                                   306, 305                               
                                           32.65                          
                                               2.70                       
                                                   4.14                   
                 77.62 (3F, bs, CF.sub.3)                                 
                                   157     (33.23)                        
                                               (2.77)                     
                                                   (4.31)                 
                 228.0 (2F, dt, J = 45, 10.2 Hz,                          
                 CH.sub.2 F)                                              
56     193-195   -54.75 (1F, bs, NF)                                      
                                   375     24.9                           
                                               0.85                       
                                                   3.64                   
                 61.50 (6F, s, β-CF.sub.3)                           
                                   271     (25.08)                        
                                               (0.79)                     
                                                   (3.66)                 
                 78.00 (3F, s, CF.sub.3)                                  
                                   69                                     
57     94-96     -36.37 (1F, bs, NF)                                      
                                   361     43.63                          
                                               2.72                       
                                                   3.58                   
                 77.40 (3F, s, CF.sub.3)                                  
                                   (M.sup.+ -HF)                          
                                           (44.10)                        
                                               (2.91)                     
                                                   (3.67)                 
58     vsicous   -46.88 (1F, bs, NF)                                      
                                   241     31.17                          
                                               2.72                       
                                                   5.26                   
                 78.00 (3F, s, CF.sub.3)                                  
                                   (M.sup.+ -HF)                          
                                           (32.18)                        
                                               (2.68)                     
                                                   (5.36)                 
59     159       -15.75 (1F, bs, NF)                                      
                                   359     48.04                          
                                               6.27                       
                                                   3.68                   
                 76.87 (3F, s, NF) 338     (47.75)                        
                                               (6.14)                     
                                                   (3.71)                 
                                   190                                    
60     162-168   -15.75 (1F, bs, NF)                                      
                                   306, 305                               
                                           33.11                          
                                               2.68                       
                                                   4.20                   
                 77.68 (3F, s, CF.sub.3)                                  
                                   175, 172                               
                                           (33.23)                        
                                               (2.77)                     
                                                   (4.31)                 
                 119.3 (2F, dd, J = 52.5, 10.6 Hz,                        
                                   157, 156                               
                 CHF.sub.2)                                               
61, 62 90-91     -48.75 (1F, bs, NF)                                      
                                   104     32.53                          
                                               2.64                       
                                                   7.43                   
                 149.6 (4F, s, BF.sub.4)   (32.43)                        
                                               (2.70)                     
                                                   (7.57)                 
65     208-209   -52.67 (1F, bs, NF)                                      
                                   169                                    
                                   167(M.sup.+ -HBF.sub.4)                
                                           23.62                          
                                               1.11                       
                                                   5.44                   
                 150.5 (4F, s, BF.sub.4)                                  
                                   165     (23.66)                        
                                               (1.19)                     
                                                   (5.52)                 
__________________________________________________________________________
The Following Examples 66-133 are contemplated to elucidate the use of the compounds according to the present invention as the fluorine introducing agent.
EXAMPLE 66 ##STR127##
A methylene chloride solution (1 ml) containing 1.0 mmole of phenol and 1.0 mmole of N-fluoro-3,5-dichloropyridinium trifluyoromethanesulfonate was refluxed under an argon atmosphere for 5 hours. After the reaction was completed, the reaction solution was analysed by gas chromatography to reveal that it contained o-fluorophenol (0.44 mmole), p-fluorophenol (0.13 mmole), 2,4-difluorophenol (0.06 mmole), and phenol (0.27 mmole). Thus the yields of o-fluorophenol, p-fluorophenol and 2,4-difluorophenol were 60%, 18%, and 7% respectively. The total yield was 88% corresponding to the total conversion of 73%. It is noted that no m-fluorophenol was formed.
EXAMPLE 67 ##STR128##
A 1,1,2-trichloroethane solution (2 ml) containing 1.0 mmole of phenol and 0.5 mmole of N-fluoropyriinium trifluoromethanesulfonate was heated at 100° C. for 24 hours under an argon atmosphere and 0.25 mmole of additional N-fluoropyridinium trifluoromethanesulfonate, was added both after 3 hours and 6 hours, thus bringing the total amount of N-fluoropyridinium trifluoromethanesulfonate to 1.0 mmole. After the reaction, the resulting reaction solution was subjected to gas chromatography to reveal that it contained 0.40 mmole of o-fluorophenol, 0.14 mmole of p-fluorophenol, 0.05 mmole of 2,4-difluorophenol and 0.21 mmole of phenol. Therefore, the yields of o-, p-fluorophenols and 2,4-difluoro-phenol were 51%, 18% and 6% respectively, corresponding to the total yields to 75%, with the total conversion of 79%.
EXAMPLES 68-133
A wide variety of fluorine- containing compounds were prepared by reacting N-fluoropyridinium salts according to the present invention with an equi-molar amount of compounds contemplated to be fluorinated. These examples were carried out similar to Example 66 with the reaction conditions set forth in Tables 7-10. The results obtained are also indicated in Tables 7-10. The identification of the structures of the resulting compounds were effected by comparing those with a standard specimem or with spectroscopy.
In Tables 7-10, the N-fluoropydinium salts set foth below were expressed, for simplicity' sake, with the following No. of compounds: ##STR129##
TABLE 7
    N-Fluoropyridinium     Fluorine  .sup.19 F-NMR (ppm) Example  salt
 (indicated by  Temperature Hours Conversion containing Yield (CFCl.sub.3
 internal No. Aromatic Compound compound number) Solvent (°C.) (b)
 (%) compound (%) standard in CDCl.sub.3
   68 phenol 3 CH.sub.2 CH.sub.2 room temp 18 78 o-fluorophenol 30 --
    p-fluorophenol 24 --        2,4-difluorophenol  3 -- 69 phenol 4
 CH.sub.2 CH.sub.2 reflux temp
  5  o-fluorophenol 40 --        p-fluorophenol 11        2,4-difluorophen
 ol  5 -- 70 phenol 5 CH.sub.2 ClCHCl.sub.2 100 16 80 o-fluorophenol 49
 --        p-fluorophenol 14 --        2,4-difluorophenol trace -- 71
 phenol 6 CH.sub.2 ClCHCl.sub.2 reflux temp 72 73 o-fluorophenol 24 -- 72
 phenol 7 CH.sub.2 ClCHCl.sub. 2 100 24 75 o-fluorophenol 47 --
 p-fluorophenol 31 --        2,4-difluorophenol  3 -- 73 phenol 14
 CH.sub.2
  Cl.sub.2 reflux temp 24 61 o-fluorophenol 84 --        p-fluorophenol
 10 --        2,4-difluorophenol  1 -- 74 phenol 16 CH.sub.2 ClCHCl.sub.2
 120 10 70 o-fluorophenol 45 --        p-fluorophenol 15 -- 75 phenol 17
 CH.sub.2
  ClCHCl.sub.2 120 10 70 o-fluorophenol 42 --        p-fluorophenol 15 --
 76 anisole 2 CH.sub.2 ClCH.sub.2 Cl reflux temp 18 65 o-fluoroanisole 48
 --        p-fluoroanisole 51 -- 77 anisole 1 CH.sub.2 ClCH.sub.2 Cl
 reflux temp 18 58 o-fluoroanisole 40 --        p-fluoroanisole 47 -- 78
 anisole 3 CH.sub.2 Cl.sub.2 reflux temp 24 71 o-fluoroanisole 44 --
   p-fluoroanisole 48 --
   79
  2 CH.sub.2
  Cl.sub.2 reflux temp 5 57
 ##STR130##
  71 140.3
  80
 ##STR131##
  3 CH.sub.2
  Cl.sub.2 reflux temp 3 79
 ##STR132##
  46 140.3
  ##STR133##
  23 149.6
  81
 ##STR134##
  18 CH.sub.2
  Cl.sub.2 reflux temp 50 85
 ##STR135##
  55 140.3
  82
 ##STR136##
  2 CH.sub.2
  Cl.sub.2 reflux temp 47 78
 ##STR137##
  51 140.3
  83
 ##STR138##
  3 CH.sub.2
  Cl.sub.2 reflux temp 25 62
 ##STR139##
  47 134.6
  ##STR140##
  31 149.6
  84
 ##STR141##
  3 CH.sub.2
  Cl.sub.2 reflux temp 48 53
 ##STR142##
  28 130.5
  ##STR143##
  24 117.8
  85
 ##STR144##
  3 CH.sub.2
  Cl.sub.2 reflux temp 32 68
 ##STR145##
  47 131.9
  ##STR146##
  32 119.1
  ##STR147##
  5 1158126.7
  86
 ##STR148##
  2 CH.sub.2
  Cl.sub.2 reflux temp 18 56
 ##STR149##
  71 133.1  87 p t butyphenol 2 CH.sub.2 Cl.sub.2 reflux temp 27 83
 2-fluoro-4,1- 68 139.1        butylphenol        p-fluorophenol  7 123.5
 88 2 naphthol 2 CH.sub.2 Cl.sub.2 room temp 26 80 1-fluoro-2- 84 155.2
      naphthol
  ##STR150##
  11 101.6  89 benzene 3 benzene reflux temp 24 -- fluorobenzene 56 111.4
          (in benzene solvent)

TABLE 8
    N-Fluoropyridinium    Fluorine  .sup.19 F-NMR (ppm) Example  salt
 (indicated by  Temperature Hours Containing Yield (CFCl.sub.3 internal
 No. Enol Compound compound number) Solvent (°C.) (h) compound (%)
 standard in CDCl.sub.3)
            90
  ##STR151##
  1 CH.sub.2
  Cl.sub.2 room temp 7
 ##STR152##
  87 188(d, J=50Hz)
  91
 ##STR153##
  7 CH.sub.2
  Cl.sub.2 room temp 4
 ##STR154##
  57 188(d, J=50Hz)
  92
 ##STR155##
  8 CH.sub.2
  CH.sub.2 room temp 3
 ##STR156##
  65 188(d, J=50Hz)
  93
 ##STR157##
  2 CH.sub.2
  Cl.sub.2 room temp 2
 ##STR158##
  62 188(d, J=50Hz)
  94
 ##STR159##
  6 CH.sub.2
  Cl.sub.2 reflux temp 6
 ##STR160##
  41 188(d, J=50Hz)
  95
 ##STR161##
  9 CH.sub.2
  CH.sub.2 reflux temp 8
 ##STR162##
  23 188(d, J=50Hz)
  96
 ##STR163##
  5 CH.sub.2
  Cl.sub.2 room temp 5
 ##STR164##
  69 188(d, J=50Hz)
  97
 ##STR165##
  10 CH.sub.2
  Cl.sub.2 reflux temp 24
 ##STR166##
  40 188(d, J=50Hz)
  98
 ##STR167##
  3 CH.sub.2
  Cl.sub.2 reflux temp 3
 ##STR168##
  24 188(d, J=50Hz)
  99
 ##STR169##
  1 CH.sub.2 Cl.sub.2 room temp 2 PhCHFCOOEt 65 180(d, J=48Hz)  100
  ##STR170##
  7 CH.sub.2 Cl.sub.2 room temp 2 PhCHFCOOEt 71 180(d, J=48Hz)  101
  ##STR171##
  7 CH.sub.2 Cl.sub.2 room temp 2 PhCHFCOOH 68 181(d, J=48Hz)  102
  ##STR172##
  11 CH.sub.2 Cl.sub.2 room temp 2 PhCHFCOOH 70 181(d, J=48Hz)  103
  ##STR173##
  1 CH.sub.2
  Cl.sub.2 reflux temp 3
 ##STR174##
  58 188(m)
  104
 ##STR175##
  1 CH.sub.2
  Cl.sub.2 room temp 3
 ##STR176##
  31 168(t, J=51Hz)
  ##STR177##
  21 184(d, J=50Hz)
  ##STR178##
  10 206(d, J=50Hz)
  105
 ##STR179##
  1 CH.sub.2
  Cl.sub.2 room temp 1
 ##STR180##
  31 166(t, J=50Hz)
  ##STR181##
  11 183(d, J=50Hz)
  ##STR182##
  18 206(d, J=50Hz)
  106
 ##STR183##
  1 CH.sub.2
  Cl.sub.2 reflux temp 10
 ##STR184##
  48 166(t, J=48Hz)
  ##STR185##
  24 184(d, J=48Hz)
  107
 ##STR186##
  1 CH.sub.2
  Cl.sub.2 reflux temp 14
 ##STR187##
  31 166(t, J=49.5Hz)
  ##STR188##
  20 183(d, J=50Hz)
  108
 ##STR189##
  1 CH.sub.2
  Cl.sub.2 reflux temp 2
 ##STR190##
  59 192(m)
  109
 ##STR191##
  15 CH.sub.2 CH.sub.2 CH.sub.3
  CN(4/1) 15 1
 ##STR192##
  63 138(s)
  110
 ##STR193##
  2 CH.sub.2
  Cl.sub.2 reflux temp 24
 ##STR194##
  72 163(t, J=20Hz)
  111
 ##STR195##
  7 CH.sub.2
  Cl.sub.2 reflux temp 48
 ##STR196##
  83 163(t, J=20Hz)
  112
 ##STR197##
  12 CH.sub.2
  Cl.sub.2 reflux temp 48
 ##STR198##
  68 163(t, J=20Hz)
  113
 ##STR199##
  2 CH.sub.2
  Cl.sub.2 reflux temp. 15
 ##STR200##
  48 171(q, J=28Hz)
  114
 ##STR201##
  1 CH.sub.2
  Cl.sub.2 reflux temp 0.4
 ##STR202##
  59 177(m)
 *the reaction product was hydrorized in a DMFconc. HCl aqueous soln (R1)

                                  TABLE 9                                 
__________________________________________________________________________
Ex-                                                                       
am-           N-Fluoropyndinium                                           
                           Temper-                  .sup.19 F-NMR(ppm)    
ple           salt (indicated by                                          
                        Sol-                                              
                           ature Hours                                    
                                     Fluorine containing                  
                                                Yield                     
                                                    (CFCl.sub.3 internal  
No.                                                                       
   Carbon anion                                                           
              compound number)                                            
                        vent                                              
                           (°C.)                                   
                                 (h) compound   (%) standard in           
                                                    CDCl.sub.3)           
__________________________________________________________________________
115                                                                       
    ##STR203##                                                            
              7         THF                                               
                           room temp.                                     
                                 0.17                                     
                                      ##STR204##                          
                                                78  162.8(t, J=20.3Hz)    
116                                                                       
    ##STR205##                                                            
              7         THF                                               
                           room temp.                                     
                                 1                                        
                                      ##STR206##                          
                                                44  172.5(q, J=22.5Hz)    
117                                                                       
    ##STR207##                                                            
              7         THF                                               
                           0     0.17                                     
                                      ##STR208##                          
                                                78  158.0(q, J=21.9Hz)    
118                                                                       
    ##STR209##                                                            
              7         THF                                               
                           0                                              
                                      ##STR210##                          
                                                42  144.6(q, J=48.6Hz)    
                                      ##STR211##                          
                                                 6  111.0(s)              
119                                                                       
    ##STR212##                                                            
              7         THF                                               
                           0- room temp.                                  
                                 0.17                                     
                                      ##STR213##                          
                                                71  118.9(s)              
120                                                                       
   n-C.sub.12 H.sub.25 MgCl                                               
              7         Et.sub.2 O                                        
                           0     0.5 n-C.sub.12 H.sub.25 F                
                                                75  210.8(tt, J=51.3,     
                                                    17Hz)                 
121                                                                       
   PhMgCl     7         THF                                               
                           0     0.17                                     
                                     PhF        58  --                    
122                                                                       
    ##STR214##                                                            
              7         THF                                               
                           0     1                                        
                                      ##STR215##                          
                                                50  179.6(d,              
__________________________________________________________________________
                                                    J=49.6Hz)             

TABLE 10
    N-Fluoropyridinium      F-NMR (ppm) Example  salt (indicated by
 Temperature Hours  Yield (CFCl.sub.3 internal standard) No. Sulfide
 compound number) Solvent (°C.) (h) α
 fluorosulfide (%) Solvent 182.8(t, 52.5Hz)
             123
  ##STR216##
  7 CH.sub.2
  Cl.sub.2 room temp. 8
 ##STR217##
  87 CDCl.sub.3 182.8(t, 52.5Hz)
  124
 ##STR218##
  1 CH.sub.2
  Cl.sub.2 room temp. 75
 ##STR219##
  48 CDCl.sub.3 182.8(t, 52.5Hz)  125 PhSCH.sub.3 7 CH.sub.2 Cl.sub.2
 room temp. 4 PhSCH.sub.2 F 85 CDCl.sub.3 180.3(t, 54Hz)  126 PhSCH.sub.3
 1 CH.sub.2 Cl.sub.2 room temp. 6 PhSCH.sub.2 F 56 CDCl.sub.3 180.3(t,
 54Hz)  127 PhCH.sub.2 SCH.sub.3 7 CH.sub.2 Cl.sub.2 room temp. 1
  ##STR220##
  76 CH.sub.2 Cl.sub.2 CH.sub.2 Cl.sub.2 152.0(d, 56Hz)187.2(t, 51Hz)
 128 PhCH.sub.2 SCH.sub.3 7 CH.sub.2
  Cl.sub.2 0 3
 ##STR221##
  48 CH.sub.2 Cl.sub.2 CH.sub.2 Cl.sub.2 152.0(d, 56Hz)187.2(t, 51Hz)
 129 n-C.sub.12 H.sub.25 SCH.sub.3 7 CH.sub.2 Cl.sub.2 room temp. 175
 n-C.sub.12 H.sub.25 SCH.sub.2 F 41 CH.sub.2 Cl.sub.2 184.2(t, 52Hz)  130
 CH.sub.3 SCH.sub.2 COOEt 7 CH.sub.2 Cl.sub.2 room temp. 10 CH.sub.1
 SCHFCOOEt 48 CH.sub.2 Cl.sub.2 167.3(d, 54Hz)
  131
 ##STR222##
  7 CH.sub.2
  Cl.sub.2 room temp. 75
 ##STR223##
   40 CDCl.sub.2 183.8(t, 51Hz)
  132
 ##STR224##
  13 CH.sub.2
  Cl.sub.2 40 4.5
 ##STR225##
  75 CDCl.sub.3 182.8(t, 52.5Hz)  133 PhSC.sub.2 COOMe 7 CH.sub.2
 Cl.sub.2 room temp. 23 PhSCHFCOOMe 45 CDCl.sub.3 158.4(d, 52Hz)

Claims (5)

What is claimed is:
1. A N-fluoropyridinium salt having the general formula: ##STR226## wherein: (a) R1 through R5 are each a group selected from the class consisting of hydrogen, halogen, and methyl;
(b) when at least two of each of R1 through R5 are hydrogen, then the remaining one through three groups of R1 through R5 can each be selected from the class consisting of:
phenylcarbonyloxy substituted methyl,
a mixture of at least one fluoro substituted methyl group and at least one group selected from the class consisting of methyl, trifluoromethyl and halogen, and
tertiary butyl or a mixture of methyl and t-butyl provided that, when at least two of each of R1 through R5 are tertiary butyl, said tertiary butyl groups are not adjacent;
(c) when at least three of each of R1 through R5 are hydrogen, then the remaining one or two groups of R1 through R5 can each be selected from the class consisting of:
phenyl,
acetyl,
alkoxycarbonyl containing a total of 2 through 5 carbon atoms wherein said aklyl substitute contains a total of 1 through 4 carbon atoms,
nitro
cyano,
alkoxy containing 1 through 10 carbon atoms, and acyloxy wherein said acyl group contains 1 through 4 carbon atoms;
(d) when R3 is hydrogen, then R1 and R2 taken together and R4 and R5 taken together can each form a six-membered carbocyclic ring which is inclusive of two adjacent carbon atoms of the pyridine ring; .[.and.]. .Iadd.or .Iaddend.
(e) when R3 and R5 are each hydrogen, then R1 and R2 taken together can form a five-membered heterocyclic ring which contains one oxygen atom, which is inclusive of two carbon atoms of the pyridine ring, and which has an oxo oxygen atom substituted on each ring carbon atom adjacent said ring oxy oxygen atom; and
(f) X is a conjugate base of a .[.Brosted.]. .Iadd.Bronsted .Iaddend.acid except for halides, .Iadd.provided that said N-fluoropyridinium salt is not N-fluoropyridinium hexafluoroantimonate, N-fluoropyridinium hexafluoroarsenate, or N-fluoropyridinium hexafluoroiodate. .Iaddend.
2. The N-fluoropyridinium salt of claim 1 wherein X is selected from the class consisiting of: --OSO2 CF3, --PF6, .[.SbF6, .]. --ClO4, --OSO2 F, --OSO2 CH3, ##STR227##
3. A process for making an N-fluoropyridinium salt comprising reacting fluorine, a Bronsted acid containing a conjugate base except for haldies, and a pyridine compound in a reaction solvent, said pyridine compound having a general formula: ##STR228## wherein: (a) R1 through R5 are each a group selected from the class consisting of hydrogen, halogen, and methyl;
(b) when at least two of each of R1 through R5 are hydrogen, then the remaining one through three groups of R1 through R5 can each be selected from the class consisting of:
phenylcarbonyloxy substituted methyl,
a mixture of at least one fluoro substitutedmethyl group and at least one group selected from the class consisting of methyl, trifluoromethyl and halogen, and
alkyl containing two through four carbon atoms, provided that when each of two of R1 through R5 are tertiary butyl, said tertiary butyl groups are not adjacent; and
(c) when at least three of R1 through R5 are each hydrogen, then the remaining one or two groups of R1 through R5 can each be selected from the class consisting of:
phenyl,
acetyl,
alkoxycarbonyl containing a total of 2 through 4 carbon atoms wherein said alkyl substitutent contains a total of 1 through 4 carbon atoms,
nitro,
cyano,
alkoxy containing 1 through 10 carbon atoms, and acyloxy wherein said acyl group contains 1 through 4 carbon atoms;
(d) when R3 is hydrogen, then R1 and R2 taken together and R4 and R5 taken together can each form a six-membered carbocyclic ring which is inclusive of two adjacent carbon atoms of the pyridine ring; .[.and.]. .Iadd.or .Iaddend.
(e) when R3 through R5 are each hydrogen, then R1 and R2 taken together can form a five-membered heterocyclic ring which contains one oxygen atom, which is inclusive of two carbon atoms of the pyridine ring, and which has an oxo oxygen atom substituted on each ring carbon atom adjacent said ring oxy oxygen atom, .Iadd.provided that said conjugate base is not -- SbF6, -- AsF6 , or -- IF6, when R1, R2, R3, R4, and R5 are each hydrogen. .Iaddend.
4. The process of claim 3 wherein said reaction solvent is selected from the class consisting of acetonitrile, methylene chloride, chloroform, tri-chloromethane, trichlorofluoromethane, trichlorotrifluoromethane, ethyl acetate, diethyl ether, tetrahydrofuran and mixtures thereof at a temperature in the range of about -100° C. to about 40° C., while maintaining the molar ratio of said Bronsted acid to said pyridine compound at least about 1:1, and wherein the molar ratio of said fluorine to said pyridine compound is at least about 1:1.
5. The process of claim 3 wherein said .[.Brosted.]. .Iadd.Bronsted .Iaddend.acid conjugate base is selected from the class consisting of: ##STR229##
US08/197,711 1985-06-03 1994-02-17 N-fluoropyridinium salt and process for preparing same Expired - Lifetime USRE35177E (en)

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US2227587A 1987-03-05 1987-03-05
US07/296,411 US4996320A (en) 1985-06-03 1989-01-09 N-fluoropyridinium salt and process for preparing same
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Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0204535A1 (en) * 1985-06-03 1986-12-10 Sagami Chemical Research Center N-fluoropyridinium salt and process for preparing same

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0204535A1 (en) * 1985-06-03 1986-12-10 Sagami Chemical Research Center N-fluoropyridinium salt and process for preparing same

Non-Patent Citations (10)

* Cited by examiner, † Cited by third party
Title
"Pyridine and Its derivatives" vol. 14, Supplement Parts 1-4 Edited by R. A. Abramovitch (1974 Parts 1-3), (1975 Part 4), John Wiley and Sons Publishers New York N.Y.
"The Chemistry of Heterocyclic Compounds a Series of Monograms" Arnold Weissberger, Consulting Editor, vol. 14, Pyridine and Its Derivatives, Parts 1-4, Edited by Erwin Clingsbert, (1960-1964) Interscience Publishers Inc., New York, N.Y.
Hasso Meinert, Habilitationsschrift, "Contributions of the Chemistry of Halogen Fluroides, Halogens in a Positive Oxidation State and Noble Gases", Dept. of Mathematics and Natural Sciences, Humbolt Univ. Berlin, Germany Dec. 11, 1968.
Hasso Meinert, Habilitationsschrift, Contributions of the Chemistry of Halogen Fluroides, Halogens in a Positive Oxidation State and Noble Gases , Dept. of Mathematics and Natural Sciences, Humbolt Univ. Berlin, Germany Dec. 11, 1968. *
March, Advanced Organic Chemistry, Reactions, Mechanisms and Structure, Second Edition, pp. 460 468, McGraw Hill Publishers (1977). *
March, Advanced Organic Chemistry, Reactions, Mechanisms and Structure, Second Edition, pp. 460-468, McGraw-Hill Publishers (1977).
Pyridine and Its derivatives vol. 14, Supplement Parts 1 4 Edited by R. A. Abramovitch (1974 Parts 1 3), (1975 Part 4), John Wiley and Sons Publishers New York N.Y. *
Pyridine and Its Derivatives, vol. 14, Supplement Part 5, Edited by George R. Newkome, 1984, John Wiley and Sons, Inc Publishers. *
The Chemistry of Heterocyclic Compounds a Series of Monograms Arnold Weissberger, Consulting Editor, vol. 14, Pyridine and Its Derivatives, Parts 1 4, Edited by Erwin Clingsbert, (1960 1964) Interscience Publishers Inc., New York, N.Y. *
Umemoto et al, Chemical Abstracts, vol. 106(15) Abst. No. 106:119,640f Apr. 13, 1987. *

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