CA2454603A1 - Process for preparing 4-aminodiphenylamine - Google Patents
Process for preparing 4-aminodiphenylamine Download PDFInfo
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- CA2454603A1 CA2454603A1 CA002454603A CA2454603A CA2454603A1 CA 2454603 A1 CA2454603 A1 CA 2454603A1 CA 002454603 A CA002454603 A CA 002454603A CA 2454603 A CA2454603 A CA 2454603A CA 2454603 A1 CA2454603 A1 CA 2454603A1
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- nitrobenzene
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/68—Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/30—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds
- C07C209/32—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds by reduction of nitro groups
- C07C209/36—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds by reduction of nitro groups by reduction of nitro groups bound to carbon atoms of six-membered aromatic rings in presence of hydrogen-containing gases and a catalyst
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Abstract
The invention is directed to a method of producing 4-aminodiphenylamine or substituted derivatives thereof comprising the steps of bringing an aniline or aniline derivative and nitrobenzene derivative into reactive contact; and reacting the aniline and nitrobenzene in a confined zone at a suitable time and temperature, in the presence of a mixture comprising a strong base and a suitable phase transfer catalyst and an oxidant to produce a 4- aminodiphenylamine intermediate product. Alternatively, the mixture may comprise an inorganic salt or metal organic salt having a cation that would be a suitable cation of a strong inorganic base, and an oxidant and organic bas e, the mixture not including a reaction product of betaine and a strong inorgan ic base. The aminodiphenylamine intermediate product is reduced to produce 4- aminodiphenylamine or substituted derivatives thereof.
Description
BACKGROUND OF THE INVENTION
1. Field ofi the Invention The present invention relates to a process for preparing 4-aminodiphenyl-amines intermediates.
1. Field ofi the Invention The present invention relates to a process for preparing 4-aminodiphenyl-amines intermediates.
2. Related Art 4-Aminodiphenylamines are widely used as intermediates in the manufacture of alkylated derivatives having utility as antiozonants and antioxidants, as stabilizers for monomers and polymers, and in various specialty applications. For example, reductive alkylation of 4-aminodiphenylamine (4-ADPA) with methylisobutyl ketone provides N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylene-diamine, which is a useful antiozonant for the protection of various rubber products.
4-Aminodiphenylamine derivatives can be prepared in various ways. An attractive synthesis is the reaction of an optionally substituted aniline with an optionally substituted nitrobenzene in the presence of a base, as disclosed, for example, in U.S. 5,608,111 (to Stern et al.) and U.S. 5,739,403 (to Reinartz et al.).
U.S. 5,608,111 describes a process for the preparation of an optionally substituted 4-ADPA wherein in a first step optionally substituted aniline and optionally substituted nitrobenzene are reacted (coupled) in the presence of a base. In working examples, aniline and nitrobenzene are. reacted in the presence of tetramethylammonium hydroxide as the base, and water and aniline are azeotropically removed during the coupling reaction.
International publication WO 00/35853 discloses a method of preparation of intermediates of 4-aminodiphenylamine by the reaction of aniline with nitrobenzene in a liquid medium where the reaction system consists of a solution of salts of true zwitterions with hydroxides. A combination of potassium hydroxide and betaine hydrate is exemplified. The reaction may take place in the presence of free oxygen.
EP publication 566 783 describes a method of manufacture of 4-nitrodiphenylamine by the reaction of nitrobenzene with aniline in the medium of a polar aprotic solvent in a strongly alkaline reaction system. A phase transfer catalyst such as tetrabutylammonium hydrogen sulfate is employed. This reference requires that the reaction be carried out in an oxygen-free atmosphere in order to prevent undesirable side reactions caused by oxidation.
US Patent No. 5,117,063 and International publication WO 01/14312 disclose processes for preparing 4-nitrodiphenylamine and 4-nitrosodiphenhlamine, using an inorganic base with crown ether, a phase transfer catalyst.
US Patent No. 5,453,541 teaches that an external desiccant, such as anhydrous sodium sulfate, may be used to absorb excess water in an anaerobic or aerobic process for producing one or more 4-ADPA intermediates in which substituted aniline derivatives and nitrobenzene are brought into reactive contact.
The objective of the present invention is to provide a superior method for producing one or more 4-ADPA intermediates by reacting aniline and nitrobenzene in the presence of a strong base and a phase transfer catalyst, or in the presence of an organic base and an inorganic salt or a metal organic salt.
SUMMARY OF THE INVENTION
In brief summary, in one embodiment, the present invention is for a method of producing 4-aminodiphenylamine or substituted derivatives thereof comprising the steps of:
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact;
(b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zone at a suitable time, pressure and temperature, in the presence of a mixture comprising a strong base, an oxidant and a phase transfer catalyst selected from the group of compounds defined by:
UR4)e-Y-(R~ R2RsN+)lcX ab (Z)~
where R~, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from C~ to C2o, (R4)e is hydrogen for a = 0, R4 is R~R2R3N~ for a = 1 or 2, Y is alkyl, aryl , alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, X is an anionic moiety of the form fluoride, chloride, hydroxide, sulfate, hydrogensulfate, acetate, formate; nitrate, phosphate, hydrogen phosphate, dihydrogen phosphate, oxalate, carbonate, borate, tartrate, citrate, malonate and mixtures of said compounds, where a = the valence of the anionic moiety (1, 2 or 3), b and c are whole number integers of value 1, 2 or 3 and d is a whole number integer of value 0 to 4; and (c) reducing the 4-aminodiphenylamine intermediate product of step (b) to produce 4-aminodiphenylamine or substituted derivatives thereof.
In a second embodiment, the present invention is a method of producing 4-aminodiphenylamine or substituted derivatives thereof comprising the steps of:
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact;
(b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zorie at a suitable time, pressure and temperature in the presence of a mixture comprising an oxidant and a strong base that also functions as a phase transfer catalyst selected from the group of compounds defined by:
I(R4)e-~'-(R~R2Rsn1+)~c(OI-I)b II
( (Z)a .5 where R~, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from C~ to C2o, (R4)e is hydrogen for a = 0, R~ is R~R~R3N+ for a = 1 or 2, Y is alkyl, aryl , alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, b and c are whole number integers of value 1, 2 or 3 and d is a whole number integer of value 0 to 4; and (c) reducing the 4-aminodiphenylamine intermediate product of step (b) to produce 4-aminodiphenylamine or substituted derivatives thereof.
In a third embodiment, the present invention is a method of producing 4-aminodiphenylamine or substituted derivatives thereof comprising the steps of:
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact; and (b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zone at a suitable time, pressure and temperature, in the presence of a mixture comprising an inorganic salt or metal organic salt, or mixtures thereof, having a cation that would be a suitable cation of a strong inorganic base, an oxidant and one or more of an organic base selected from the group of compounds defined by:
UR4)e-~'-(R~ R2RsN+)1cX ab I I I
(Z)d where R~, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from 1 to about 20 carbon atoms, a is a whole number integer of value 0, 1, 2 or 3, (R4)e is hydrogen for a = 0, is R~R2R3N~ for a = 1, 2, or 3, X is an anion capable of abstracting a proton from the nitrogen of an aniline or aniline derivative, Y is alkyl, aryl , alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, where a = the valence of the anionic moiety and is a whole number integer of 1, 2, 3 or 4, b and care whole number integers of value 1, 2, 3 or 4 and d is a whole number integer of value 0, 1, 2, 3 or 4, said mixture not including a reaction product of betaine and a strong inorganic base; and (c) reducing the A.-aminodiphenylamine intermediate product of step (b) to 5 produce 4-aminodiphenylamine or substituted derivatives thereof.
Other embodiments of the present invention encompass details about reaction mixtures and ratios of ingredients, particular phase transfer catalysts and particular strong bases, all of which are hereinafter disclosed in the following discussion of each of the facets of the present invention.
DETAILED DESCRIPTION OF THE INVENTION
The present invention is directed to a method, as described above, for making intermediates of 4-ADPA that has superior yield and selectivity for those intermediates. Such intermediates comprise 4-nitroso- andlor 4-nitrodiphenylamines (p-NDPA and 4-NDPA, respectively) and salts thereof. The intermediates may then be hydrogenated to produce 4-aminodiphenylamine.
An example of a substituted and multifunctional phase transfer catalyst that is consistent with the above formula 1 is (2S, 3S)-bis(trimethylammonio)-1,4-butanediol dichloride. Other effective phase transfer catalysts fitting formula I, in addition to those shown in the following examples, can be derived from examples in the literature, such as C. M. Starks and C. Liotta, Phase Transfer Catalysis, Principles and Techniques, Academic Press, 1978 and W. E. Kelley, Fluka-Compendium, Vol. 1,2,3, Georg Thieme Verlag, New York, 1986, 1987, 1992.
An example of a substituted and multifunctional organic base that is consistent with the above formulas II and III is (2S, 3S)-bis(trimethylammonio)-1,4-butanediol dihydroxide. Other effective organic bases fitting formulas 1l and III, in addition to those shown in the following examples, can be derived from the above phase transfer catalysts, wherein the anion is replaced by hydroxide or other suitable anion form.
4-Aminodiphenylamine derivatives can be prepared in various ways. An attractive synthesis is the reaction of an optionally substituted aniline with an optionally substituted nitrobenzene in the presence of a base, as disclosed, for example, in U.S. 5,608,111 (to Stern et al.) and U.S. 5,739,403 (to Reinartz et al.).
U.S. 5,608,111 describes a process for the preparation of an optionally substituted 4-ADPA wherein in a first step optionally substituted aniline and optionally substituted nitrobenzene are reacted (coupled) in the presence of a base. In working examples, aniline and nitrobenzene are. reacted in the presence of tetramethylammonium hydroxide as the base, and water and aniline are azeotropically removed during the coupling reaction.
International publication WO 00/35853 discloses a method of preparation of intermediates of 4-aminodiphenylamine by the reaction of aniline with nitrobenzene in a liquid medium where the reaction system consists of a solution of salts of true zwitterions with hydroxides. A combination of potassium hydroxide and betaine hydrate is exemplified. The reaction may take place in the presence of free oxygen.
EP publication 566 783 describes a method of manufacture of 4-nitrodiphenylamine by the reaction of nitrobenzene with aniline in the medium of a polar aprotic solvent in a strongly alkaline reaction system. A phase transfer catalyst such as tetrabutylammonium hydrogen sulfate is employed. This reference requires that the reaction be carried out in an oxygen-free atmosphere in order to prevent undesirable side reactions caused by oxidation.
US Patent No. 5,117,063 and International publication WO 01/14312 disclose processes for preparing 4-nitrodiphenylamine and 4-nitrosodiphenhlamine, using an inorganic base with crown ether, a phase transfer catalyst.
US Patent No. 5,453,541 teaches that an external desiccant, such as anhydrous sodium sulfate, may be used to absorb excess water in an anaerobic or aerobic process for producing one or more 4-ADPA intermediates in which substituted aniline derivatives and nitrobenzene are brought into reactive contact.
The objective of the present invention is to provide a superior method for producing one or more 4-ADPA intermediates by reacting aniline and nitrobenzene in the presence of a strong base and a phase transfer catalyst, or in the presence of an organic base and an inorganic salt or a metal organic salt.
SUMMARY OF THE INVENTION
In brief summary, in one embodiment, the present invention is for a method of producing 4-aminodiphenylamine or substituted derivatives thereof comprising the steps of:
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact;
(b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zone at a suitable time, pressure and temperature, in the presence of a mixture comprising a strong base, an oxidant and a phase transfer catalyst selected from the group of compounds defined by:
UR4)e-Y-(R~ R2RsN+)lcX ab (Z)~
where R~, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from C~ to C2o, (R4)e is hydrogen for a = 0, R4 is R~R2R3N~ for a = 1 or 2, Y is alkyl, aryl , alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, X is an anionic moiety of the form fluoride, chloride, hydroxide, sulfate, hydrogensulfate, acetate, formate; nitrate, phosphate, hydrogen phosphate, dihydrogen phosphate, oxalate, carbonate, borate, tartrate, citrate, malonate and mixtures of said compounds, where a = the valence of the anionic moiety (1, 2 or 3), b and c are whole number integers of value 1, 2 or 3 and d is a whole number integer of value 0 to 4; and (c) reducing the 4-aminodiphenylamine intermediate product of step (b) to produce 4-aminodiphenylamine or substituted derivatives thereof.
In a second embodiment, the present invention is a method of producing 4-aminodiphenylamine or substituted derivatives thereof comprising the steps of:
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact;
(b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zorie at a suitable time, pressure and temperature in the presence of a mixture comprising an oxidant and a strong base that also functions as a phase transfer catalyst selected from the group of compounds defined by:
I(R4)e-~'-(R~R2Rsn1+)~c(OI-I)b II
( (Z)a .5 where R~, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from C~ to C2o, (R4)e is hydrogen for a = 0, R~ is R~R~R3N+ for a = 1 or 2, Y is alkyl, aryl , alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, b and c are whole number integers of value 1, 2 or 3 and d is a whole number integer of value 0 to 4; and (c) reducing the 4-aminodiphenylamine intermediate product of step (b) to produce 4-aminodiphenylamine or substituted derivatives thereof.
In a third embodiment, the present invention is a method of producing 4-aminodiphenylamine or substituted derivatives thereof comprising the steps of:
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact; and (b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zone at a suitable time, pressure and temperature, in the presence of a mixture comprising an inorganic salt or metal organic salt, or mixtures thereof, having a cation that would be a suitable cation of a strong inorganic base, an oxidant and one or more of an organic base selected from the group of compounds defined by:
UR4)e-~'-(R~ R2RsN+)1cX ab I I I
(Z)d where R~, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from 1 to about 20 carbon atoms, a is a whole number integer of value 0, 1, 2 or 3, (R4)e is hydrogen for a = 0, is R~R2R3N~ for a = 1, 2, or 3, X is an anion capable of abstracting a proton from the nitrogen of an aniline or aniline derivative, Y is alkyl, aryl , alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, where a = the valence of the anionic moiety and is a whole number integer of 1, 2, 3 or 4, b and care whole number integers of value 1, 2, 3 or 4 and d is a whole number integer of value 0, 1, 2, 3 or 4, said mixture not including a reaction product of betaine and a strong inorganic base; and (c) reducing the A.-aminodiphenylamine intermediate product of step (b) to 5 produce 4-aminodiphenylamine or substituted derivatives thereof.
Other embodiments of the present invention encompass details about reaction mixtures and ratios of ingredients, particular phase transfer catalysts and particular strong bases, all of which are hereinafter disclosed in the following discussion of each of the facets of the present invention.
DETAILED DESCRIPTION OF THE INVENTION
The present invention is directed to a method, as described above, for making intermediates of 4-ADPA that has superior yield and selectivity for those intermediates. Such intermediates comprise 4-nitroso- andlor 4-nitrodiphenylamines (p-NDPA and 4-NDPA, respectively) and salts thereof. The intermediates may then be hydrogenated to produce 4-aminodiphenylamine.
An example of a substituted and multifunctional phase transfer catalyst that is consistent with the above formula 1 is (2S, 3S)-bis(trimethylammonio)-1,4-butanediol dichloride. Other effective phase transfer catalysts fitting formula I, in addition to those shown in the following examples, can be derived from examples in the literature, such as C. M. Starks and C. Liotta, Phase Transfer Catalysis, Principles and Techniques, Academic Press, 1978 and W. E. Kelley, Fluka-Compendium, Vol. 1,2,3, Georg Thieme Verlag, New York, 1986, 1987, 1992.
An example of a substituted and multifunctional organic base that is consistent with the above formulas II and III is (2S, 3S)-bis(trimethylammonio)-1,4-butanediol dihydroxide. Other effective organic bases fitting formulas 1l and III, in addition to those shown in the following examples, can be derived from the above phase transfer catalysts, wherein the anion is replaced by hydroxide or other suitable anion form.
Phase transfer catalysts known or believed to be particularly effective in the method of the invention include tetramethylammonium chloride, tetramethylammonium fluoride, tetramethylammonium hydroxide, bis-tetramethylammonium carbonate, tetramethylammonium formate and tetramethylammonium acetate; tetrabutylammonium hydrogensulfate and tetrabutylammonium sulfate; methyltributylammonium chloride; and benzyltrimethylammonium hydroxide (Triton B), tricaprylmethylammonium chloride (Aliquat 336), tetrabutylammonium chloride, tetramethylammonium nitrate, cetyltrimethylammonium chloride and choline hydroxide .
Phase transfer catalysts of the present invention have several advantages over crown ethers, such as 18-crown-6, which were described as effective with alkali metal hydroxides in references such as US Patent No. 5,117,063 and International publication WO 01/14312 discussed above. The most obvious disadvantages of crown ethers are very high initial cost and high toxicity. In addition, most crown ethers have poor solubility in water, so they cannot be recovered for recycle with an aqueous base stream. Furthermore, the boiling points of crown ethers are high enough that they cannot be recovered by distillation without an extra distillation step. Even for the class of crown ethers that have good solubility in water, solubility in organics is also good, so that there will be a high loss to the organic product stream. Finally, crown ethers are known chelating agents, so that there is a high probability of unacceptable loss of expensive hydrogenation catalyst metal, due to complexation with the crown ether.
In the method of the invention, the molar ratio of phase transfer catalyst to nitrobenzene reactant is preferably from about 0.05:1 to about 1.2:1.
The method of the present invention may also start with an organic base and an inorganic salt or a metal organic salt as in the above third embodiment.
The organic base is defined by formula Ilf in that embodiment.
Phase transfer catalysts of the present invention have several advantages over crown ethers, such as 18-crown-6, which were described as effective with alkali metal hydroxides in references such as US Patent No. 5,117,063 and International publication WO 01/14312 discussed above. The most obvious disadvantages of crown ethers are very high initial cost and high toxicity. In addition, most crown ethers have poor solubility in water, so they cannot be recovered for recycle with an aqueous base stream. Furthermore, the boiling points of crown ethers are high enough that they cannot be recovered by distillation without an extra distillation step. Even for the class of crown ethers that have good solubility in water, solubility in organics is also good, so that there will be a high loss to the organic product stream. Finally, crown ethers are known chelating agents, so that there is a high probability of unacceptable loss of expensive hydrogenation catalyst metal, due to complexation with the crown ether.
In the method of the invention, the molar ratio of phase transfer catalyst to nitrobenzene reactant is preferably from about 0.05:1 to about 1.2:1.
The method of the present invention may also start with an organic base and an inorganic salt or a metal organic salt as in the above third embodiment.
The organic base is defined by formula Ilf in that embodiment.
Organic bases known or believed to be particularly effective for the second and third embodiments include quaternary ammonium hydroxides selected from the group consisting of, but not limited to, tetramethylammonium hydroxide, tetrabutylammonium hydroxide, methyltributylammonium hydroxide, benzyltrimethylammonium hydroxide (Triton B), tricaprylmethylammonium hydroxide, cetyltrimethylammonium hydroxide and choline hydroxide, and equivalent quaternary ammonium alkoxides, acetates, carbonates, bicarbonates, cyanides, phenolics, phosphates, hydrogen phosphates, hypochlorites, borates, hydrogen borates, dihydrogen borates, sulfides, silicates, hydrogen silicates, dihydrogen silicates and trihydrogen silicates.
The term '"strong inorganic base" as used with respect to the meaning of a cation of an inorganic salt or metal organic salt is intended to mean a base that is capable of abstracting a proton from the nitrogen of an aniline or aniline derivative, and may include any base having a pKb less that about 9.4, which is the pKb of aniline. Various aniline derivatives may have different pKb values, but a pKb of about 9.4 is employed as a general guide. The base will preferably have a pKb less than about 7.4.
The term "capable of abstracting a proton from the nitrogen of an aniline or aniline derivative" as applied to anion "X" of formula III, is intended to mean an anion also having a pKb value as discussed above with respect to the strong inorganic base.
Possible anions for "X" in formula III, in addition to hydroxide, include:
alkoxide (pKb < 1), acetate (pKb = 9.25), carbonate (pKb = 3.75), bicarbonate (pK~ = 7.6), cyanide (pKb = 4.7), phenolic (pKb = 4.1 ), phosphate (pKb =
1.3), hydrogen phosphate (pKb = 6.8), hypochlorite (pKb =6.5), borate (pKb < 1 ), hydrogen borate (pKb < 1), dihydrogen borate (pKb = 4.7), sulfide (pKb = 1.1), silicate (pKb = 2), hydrogen silicate (pKa = 2), dihydrogen silicate (pKb =
2.2) and trihydrogen silicate (pKb = 4.1).
The term '"strong inorganic base" as used with respect to the meaning of a cation of an inorganic salt or metal organic salt is intended to mean a base that is capable of abstracting a proton from the nitrogen of an aniline or aniline derivative, and may include any base having a pKb less that about 9.4, which is the pKb of aniline. Various aniline derivatives may have different pKb values, but a pKb of about 9.4 is employed as a general guide. The base will preferably have a pKb less than about 7.4.
The term "capable of abstracting a proton from the nitrogen of an aniline or aniline derivative" as applied to anion "X" of formula III, is intended to mean an anion also having a pKb value as discussed above with respect to the strong inorganic base.
Possible anions for "X" in formula III, in addition to hydroxide, include:
alkoxide (pKb < 1), acetate (pKb = 9.25), carbonate (pKb = 3.75), bicarbonate (pK~ = 7.6), cyanide (pKb = 4.7), phenolic (pKb = 4.1 ), phosphate (pKb =
1.3), hydrogen phosphate (pKb = 6.8), hypochlorite (pKb =6.5), borate (pKb < 1 ), hydrogen borate (pKb < 1), dihydrogen borate (pKb = 4.7), sulfide (pKb = 1.1), silicate (pKb = 2), hydrogen silicate (pKa = 2), dihydrogen silicate (pKb =
2.2) and trihydrogen silicate (pKb = 4.1).
While aniline most effectively couples with nitrobenzene, certain aniline derivatives comprising amides such as formanilide, phenylurea and carbanilide as well as the thiocarbanilide can be substituted to produce 4-ADPA
intermediates.
Although the reactants of the method of the invention are referred to as "aniline" and "nitrobenzene", and when it is 4-ADPA that is being manufactured the reactants are in fact aniline and nitrobenzene, it is understood that the reactants may also comprise substituted aniline and substituted nitrobenzene.
Typical examples of substituted anilines that may be used in accordance with the process of the present invention include but are not limited to 2-methoxyaniline, 4-methoxyaniline, 4-chloroaniline, p-toluidine, 4-nitroaniline, 3-bromoaniline, 3-bromo-4-aminotoluene, p-aminobenzoic acid, 2,4-diaminotoluene, 2,5-dichloroaniline, 1,4-phenylene diamine, 4,4'-methylene dianiline, 1,3,5-triaminobenzene, and mixtures thereof. Typical examples of substituted nitrobenzenes that may be used in accordance with the process of the present invention include but are not limited to o- and m-methylnitrobenzene, o- and m-ethylnitrobenzene, o- and m-methoxynitrobenzene, and mixtures thereof.
The method of the invention includes the step wherein the 4-ADPA
intermediates or substituted derivatives thereof from step (b) are subjected to a hydrogenation reaction involving the use of a hydrogenation catalyst. Details concerning choice of catalyst and other aspects of the hydrogenation reaction may be found in U.S. Patent No. 6,140,538, incorporated by reference herein.
Other means of reduction, that do not involve the direct use of hydrogen and are known to one skilled in the art, can also be used to reduce the 4-ADPA
intermediates or substituted derivatives thereof to 4-ADPA or substituted derivatives thereof.
The present invention further relates to a process for preparing alkylated derivatives of 4-aminodiphenylamines, in particular for preparing alkyl derivatives of 4-ADPA itself, which are useful for the protection of rubber products, in which process an optionally substituted aniline and an optionally substituted nitrobenzene are coupled and subsequently reduced according to the invention process, after which the 4-aminodiphenylamine so obtained is reductively alkylated to an alkylated derivative of the 4-aminodiphenylamine according to methods known to the person skilled in this technical field. Typically, the 4-ADPA
and a suitable ketone, or aldehyde, are reacted in the presence of hydrogen and platinum-on-carbon as catalyst. Suitable ketones include methylisobutyl ketone, acetone, methylisoamyl ketone, and 2-octanone. See for example U.S.
4,463,191, and Banerjee et al, J. Chem. Soc. Chem. Comm. 18, 1275-1276 (1988). Suitable catalysts can be the same as, but not limited to, those described above for obtaining the 4-ADPA.
In a preferred embodiment of the invention, the reduction is conducted in the presence of water, e.g. water is added to the reaction mixture. The use of water is particularly advantageous when the suitable base, used during the reaction of the aniline or substituted aniline derivative and the nitrobenzene or substituted nitrobenzene derivative, is water-soluble. When the base is water-soluble, the amount of water added is preferably at least the amount needed to extract the base from the organic phase. Similarly, the addition of water is also preferred for reductive alkylation, if it is carried out in the presence of the suitable base, which is water-soluble.
The molar ratio of aniline to nitrobenzene in the process according to the present invention is not particularly important, as the process will be effective with an excess of either.
Strong bases particularly effective in the first embodiment of the process of the present invention include potassium hydroxide, sodium hydroxide, cesium hydroxide, rubidium hydroxide and potassium-t-butoxide. It is preferred that mole ratio of strong base to nitrobenzene is greater than about 1:1. A particularly preferred mole ratio of strong base to nitrobenzene is about 2:1 to about 6:1.
Inorganic salts and metal organic salts that may be used in conjunction with the organic base in the third embodiment of the process of the invention have a cation that would be a suitable cation of a strong inorganic base.
These inorganic salts and metal organic salts are selected from the group consisting of, 5 but not limited to, the fluoride, chloride, bromide, sulfate, hydrogen sulfate, nitrate, phosphate, dihydrogen phosphate, formate, acetate, oxalate, malonate, citrate, tartrate, maleate, chlorate, perchlorate, chromate, rhenate and carbonate salts of cesium, rubidium, potassium and sodium. In the method of the invention, the inorganic salt or metal organic salt may be used in molar ratio to 10 nitrobenzene from about 0.05:1 to about 6.5:1.
Inorganic salts and metal organic salts known or believed to be particularly effective in the third embodiment method of the present invention are those that afford acceptable solubility for the inorganic salt or metal organic salt -organic base combination in the reaction medium, including the fluoride, chloride, bromide, sulfate, hydrogen sulfate, nitrate, phosphate, formate, acetate and carbonate salts of cesium, rubidium, potassium and sodium and mixtures thereof. It is preferred that mole ratio of organic base used with an inorganic salt or metal organic salt to nitrobenzene is greater than or equal to about 1:1.
It is also preferred that mole ratio of inorganic salt or metal organic salt to organic y base is greater than or equal to about 1:1. A particularly preferred mole ratio of organic base to nitrobenzene is about 1.1:1 to about 6:1.
It may be desirable to use a combination of an inorganic salt with a metal organic salt, two or more inorganic salts and/or two or more metal organic salts in case one of the salts that is otherwise effective for use in the process of the invention has a corrosive effect on the equipment used with the process. The combination might also provide better results than could be obtained with one salt.
The use of inorganic salts and metal organic salts with the organic base is also believed to reduce undesirable base decomposition.
intermediates.
Although the reactants of the method of the invention are referred to as "aniline" and "nitrobenzene", and when it is 4-ADPA that is being manufactured the reactants are in fact aniline and nitrobenzene, it is understood that the reactants may also comprise substituted aniline and substituted nitrobenzene.
Typical examples of substituted anilines that may be used in accordance with the process of the present invention include but are not limited to 2-methoxyaniline, 4-methoxyaniline, 4-chloroaniline, p-toluidine, 4-nitroaniline, 3-bromoaniline, 3-bromo-4-aminotoluene, p-aminobenzoic acid, 2,4-diaminotoluene, 2,5-dichloroaniline, 1,4-phenylene diamine, 4,4'-methylene dianiline, 1,3,5-triaminobenzene, and mixtures thereof. Typical examples of substituted nitrobenzenes that may be used in accordance with the process of the present invention include but are not limited to o- and m-methylnitrobenzene, o- and m-ethylnitrobenzene, o- and m-methoxynitrobenzene, and mixtures thereof.
The method of the invention includes the step wherein the 4-ADPA
intermediates or substituted derivatives thereof from step (b) are subjected to a hydrogenation reaction involving the use of a hydrogenation catalyst. Details concerning choice of catalyst and other aspects of the hydrogenation reaction may be found in U.S. Patent No. 6,140,538, incorporated by reference herein.
Other means of reduction, that do not involve the direct use of hydrogen and are known to one skilled in the art, can also be used to reduce the 4-ADPA
intermediates or substituted derivatives thereof to 4-ADPA or substituted derivatives thereof.
The present invention further relates to a process for preparing alkylated derivatives of 4-aminodiphenylamines, in particular for preparing alkyl derivatives of 4-ADPA itself, which are useful for the protection of rubber products, in which process an optionally substituted aniline and an optionally substituted nitrobenzene are coupled and subsequently reduced according to the invention process, after which the 4-aminodiphenylamine so obtained is reductively alkylated to an alkylated derivative of the 4-aminodiphenylamine according to methods known to the person skilled in this technical field. Typically, the 4-ADPA
and a suitable ketone, or aldehyde, are reacted in the presence of hydrogen and platinum-on-carbon as catalyst. Suitable ketones include methylisobutyl ketone, acetone, methylisoamyl ketone, and 2-octanone. See for example U.S.
4,463,191, and Banerjee et al, J. Chem. Soc. Chem. Comm. 18, 1275-1276 (1988). Suitable catalysts can be the same as, but not limited to, those described above for obtaining the 4-ADPA.
In a preferred embodiment of the invention, the reduction is conducted in the presence of water, e.g. water is added to the reaction mixture. The use of water is particularly advantageous when the suitable base, used during the reaction of the aniline or substituted aniline derivative and the nitrobenzene or substituted nitrobenzene derivative, is water-soluble. When the base is water-soluble, the amount of water added is preferably at least the amount needed to extract the base from the organic phase. Similarly, the addition of water is also preferred for reductive alkylation, if it is carried out in the presence of the suitable base, which is water-soluble.
The molar ratio of aniline to nitrobenzene in the process according to the present invention is not particularly important, as the process will be effective with an excess of either.
Strong bases particularly effective in the first embodiment of the process of the present invention include potassium hydroxide, sodium hydroxide, cesium hydroxide, rubidium hydroxide and potassium-t-butoxide. It is preferred that mole ratio of strong base to nitrobenzene is greater than about 1:1. A particularly preferred mole ratio of strong base to nitrobenzene is about 2:1 to about 6:1.
Inorganic salts and metal organic salts that may be used in conjunction with the organic base in the third embodiment of the process of the invention have a cation that would be a suitable cation of a strong inorganic base.
These inorganic salts and metal organic salts are selected from the group consisting of, 5 but not limited to, the fluoride, chloride, bromide, sulfate, hydrogen sulfate, nitrate, phosphate, dihydrogen phosphate, formate, acetate, oxalate, malonate, citrate, tartrate, maleate, chlorate, perchlorate, chromate, rhenate and carbonate salts of cesium, rubidium, potassium and sodium. In the method of the invention, the inorganic salt or metal organic salt may be used in molar ratio to 10 nitrobenzene from about 0.05:1 to about 6.5:1.
Inorganic salts and metal organic salts known or believed to be particularly effective in the third embodiment method of the present invention are those that afford acceptable solubility for the inorganic salt or metal organic salt -organic base combination in the reaction medium, including the fluoride, chloride, bromide, sulfate, hydrogen sulfate, nitrate, phosphate, formate, acetate and carbonate salts of cesium, rubidium, potassium and sodium and mixtures thereof. It is preferred that mole ratio of organic base used with an inorganic salt or metal organic salt to nitrobenzene is greater than or equal to about 1:1.
It is also preferred that mole ratio of inorganic salt or metal organic salt to organic y base is greater than or equal to about 1:1. A particularly preferred mole ratio of organic base to nitrobenzene is about 1.1:1 to about 6:1.
It may be desirable to use a combination of an inorganic salt with a metal organic salt, two or more inorganic salts and/or two or more metal organic salts in case one of the salts that is otherwise effective for use in the process of the invention has a corrosive effect on the equipment used with the process. The combination might also provide better results than could be obtained with one salt.
The use of inorganic salts and metal organic salts with the organic base is also believed to reduce undesirable base decomposition.
In the process according to the third embodiment of the invention, it should be noted that an organic base with an inorganic salt or a metal organic salt will give some in situ formation of the equivalent inorganic base and a phase transfer catalyst, wherein the anion in formula I for the so formed phase transfer catalyst is the anion from the salt. For example, tetramethylammonium hydroxide plus potassium bromide will give some KOH plus tetramethylammonium bromide. So the invention would include the direct use of an inorganic base with any phase transfer catalyst that can be formed in situ, such as tetramethylammonium bromide, in lieu of tetramethylammonium hydroxide and a bromide salt as separate ingredients.
A particularly preferred combination of strong base and phase transfer catalyst is potassium hydroxide and tetraalkylammonium halide. A
preferred halide is chloride. A particularly preferred combination of organic base and inorganic salt is tetraalkylammonium hydroxide and a salt in which the anion is a halide, such as potassium halide. A preferred halide anion is chloride. The above reactions would be carried out in aqueous solution with a continuous distillation of aniline-water azeotrope.
The reactive contact of the process of the first embodiment of the invention is carried out in the presence of an oxidant. The oxidant may be free oxygen, or comprise an oxidizing agent such as a peroxide, particularly hydrogen peroxide. Nitrobenzene may also function as an oxidizing agent.
In the process of the invention, the oxidant may advantageously need to be present only for part of the time during which the aniline and nitrobenzene react. Such partial oxidative conditions are particularly effective for improving selectivity. One of these instances is when an inorganic salt with a fluoride anion is employed in the reaction mixture of the third embodiment under partial oxidative conditions. It is believed that better results, conversion and selectivity, would also be obtained under partial oxidative conditions when the salt anion is sulfate, carbonate, or nitrate and other anions that give relatively low selectivity.
Another instance is when TMAH is used as a strong base that can also function as a phase transfer catalyst for the second embodiment. Moreover, although it has not been demonstrated for the first embodiment of the process of the invention, it is believed that partial oxidative conditions would also be effective for combinations of inorganic base and phase transfer catalyst that give low selectivity.
The oxidant used in the second and third embodiments of the invention may be the same as in the first embodiment.
The reactive contact may be carried out at a temperature of from about 20°C to about 150°C. Other conditions for the reactive contact include pressures in the range of from about 20 mbar to about 20 barg. Reaction time is typically less than about 3.5 hours. It is advantageous to agitate the reaction mixture during the entire reaction.
The reactions of step (b) of the first, second and third embodiments of the present method may be carried out in the presence of not greater than about 10:1 moles water to moles nitrobenzene. The amount of water does not include the water that hydrates with the reactants andlor with compounds formed in the process. When the mixture comprising a strong base and a phase transfer catalyst, or an organic base and inorganic salt or metal organic salt, is in aqueous solution, the reaction may be carried out with a continuous distillation of aniline-water azeotrope.
The first embodiment of the invention may be carried out with the phase transfer catalyst being tetramethylammonium bromide and the strong base comprising one or more inorganic bases.
The aqueous phase may be reused to form a new reaction mixture. Fresh base and phase transfer catalyst or organic base and inorganic salt or metal organic salt are added to replace losses by decomposition, by-product formation and solubility in the separated organic phase. Excess Aniline recovered by distillation from the reaction product mixture may be combined with make-up fresh aniline for recycle to form a new reaction mixture. Recovery of excess nitrobenzene is preferably carried out prior to hydrogenation of the 4-ADPA
intermediate by a separation step and the recovered nitrobenzene may be combined with make-up fresh nitrobenzene for use in the process, or hydrogenated to aniline.
The method of the present invention for the preparation of 4 aminodiphenylamines intermediates may be conducted as a batch process or may be performed continuously using means and equipment well known to the skilled person.
The reactive contact in step (a) in the first, second and third embodiments of the method of the invention may occur in a suitable solvent system. A
suitable solvent system comprises a polar aprotic solvent. The polar aprotic solvent may be selected form the group consisting of, but not limited to, dimethyl sulfoxide, benzyl ether, 1-Methyl-2-pyrrolidinone and N,N-dimethylformamide.
The invention, in its second embodiment, is a method where the strong base also functions as a phase transfer catalyst and the reaction may be in the absence of an alkali metal hydroxide. In that case the strong base/phase transfer catalyst is defined by formula II above.
The invention is illustrated by the following examples.
Experimental conditions are detailed within individual examples. In examples 1-10 the charging of reactors was performed in open air resulting in some free oxygen being present during the reactions, even when the reactor was stoppered, except for experiments, where indicated, run for comparative purposes. No attempt was made to remove water from the reaction mixtures in examples 1- 10.
In examples 11-16 a flow of air was supplied to the reactor headspace during all or part of charging reactants, heat-up to reaction temperature, nitrobenzene feed and hold, resulting in free oxygen being present during the reaction, except where indicated. Water was removed from the reaction mixture by azeotropic distillation with aniline. However, the reaction can also be effective without the azeotropic removal of water with aniline.
ANALYTICAL
Yields of individual components were determined by external standard HPLC. Approximately 0.6 grams of material to be analyzed is accurately weighed into a 50-mL volumetric flask and diluted with a buffer solution containing 39% v/v water, 36% v/v acetonitrile, 24% vlv methanol and 1 % vlv pH
7 buffer. The solution is injected through a 10 pL loop onto a reversed phase Zorbax ODS HPLC column (250 x 4.6 mm) using a binary gradient pumping system and the following elution gradient at a constant flow rate of 1.5 mL/minute:
Time, minutes %A %13 37.5 0 100 Eluent A is 75°l° vlv water, 15% v/v acetonitrife and 10%
v/v methanol.
20 Eluent B is 60% v/v acetonitrile and 40% v/v methanol. Detection is UV at nm.
Conversion for examples 1-10 is calculated by sum addition of known components plus any unknown peaks {assigned an arbitrary mole weight value of 25 216, aniline + nitrobenzene) as analyzed. In some instances, sum conversion is greater than 100% due to the formation of derivatives from aniline only.
Conversion for examples 11-16 is calculated based on the amount of, unreacted nitrobenzene remaining in the final coupling reaction mass.
Conversion is assumed to be 100% if no nitrobenzene is detected.
Selectivity is defined by the formula: (p-NDPA Yield + 4-NDPA
Yield)/(total yield). 4-NDPA is 4-nitrodiphenylamine and p-NDPA is 4-nitrosodiphenylamine. Total yield is the sum of the yield of all known and unknown peaks (assigned an arbitrary mole weight value of 216, aniline +
10 nitrobenzene).
In the tables: "An Recr" refers to compounds from which aniline may be easily recovered and is a sum total of traps-azobenzene and azoxybenzene;
"Others" are aniline and nitrobenzene coupling by-products e.g. phenazine, N-15 oxy-phenazine, 2-NDPA, 4-phenazo-diphenylamine and any unknowns.
EXPERIMENTAL
Experimental conditions are detailed within individual examples.
Example 1 illustrates that 4-ADPA intermediates may be formed from aniline and nitrobenzene in the presence of an inorganic base (potassium hydroxide) and phase transfer catalyst (tetramethylammonium chloride, TMACI) in a solvent-free system under relatively mild conditions. Yield of desired products is dependent on the amount of phase transfer catalyst added.
Aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99%, 4.97 grams, 40 mrfioles), potassium hydroxide (86% ground powder, 7.83 grams, 120 mmoles) and tetramethylammonium chloride were charged to a 50-mL round bottom flask equipped with magnetic stirrer in the amount indicated in Table 1 below. The reaction was allowed to proceed for 1 hour at 60°C in a stoppered flask. Contents were then sampled and analyzed by HPLC.
i Table 1 Yield, Conversionp-NDPA4-NDPA Other An Recr No TMACI added, KOH Only 26.3% 0.8 4.8 5,5 15.2 1.81 grams TMACI, 16 mmoles 59.2% 10.9 26.9 18.4 3.0 (0.4 vs NB) 3.62 grams TMACI, 32 mmoles 90.1 22.4 36.1 28.6 3.0 (0.8 vs NB) %
5.42 grams TMACI, 48 mmoles 98.2% 27.0 37.8 3.0 (1.2 vs NB) 30.3 7.23 grams TMACI, 64 mmoles g4,4% 26.5 36.2 28.9 2.9 (1.6 vs NB) 9.04 grams TMACI, 80 mmoles 98.9% 26.2 36.7 31.8 4.2 (2.0 vs NB) Similar results were obtained when running the reaction under slightly varying conditions (equimolar An/NB, higher reaction temperature, longer cycle time, water addition, etc.) as given below in Table 2.
Aniline (99%, 2.33 grams, 24.8 mmoles), nitrobenzene (99%, 3.08 grams, 24.8 mmoles), potassium hydroxide (86% ground powder, 9.77 grams, 150 mmoles), tetramethylammonium chloride (97%, see Table 2) and water (Table 2) were charged to a 50-mL round bottom flask equipped with magnetic stirrer. The water amount was 20% by weight of total reactor charge assuming 14% w/w H20 from KOH. The reaction was allowed to proceed for 2 hours at 80°C in an open flask. Contents were then sampled and analyzed by HPLC.
A particularly preferred combination of strong base and phase transfer catalyst is potassium hydroxide and tetraalkylammonium halide. A
preferred halide is chloride. A particularly preferred combination of organic base and inorganic salt is tetraalkylammonium hydroxide and a salt in which the anion is a halide, such as potassium halide. A preferred halide anion is chloride. The above reactions would be carried out in aqueous solution with a continuous distillation of aniline-water azeotrope.
The reactive contact of the process of the first embodiment of the invention is carried out in the presence of an oxidant. The oxidant may be free oxygen, or comprise an oxidizing agent such as a peroxide, particularly hydrogen peroxide. Nitrobenzene may also function as an oxidizing agent.
In the process of the invention, the oxidant may advantageously need to be present only for part of the time during which the aniline and nitrobenzene react. Such partial oxidative conditions are particularly effective for improving selectivity. One of these instances is when an inorganic salt with a fluoride anion is employed in the reaction mixture of the third embodiment under partial oxidative conditions. It is believed that better results, conversion and selectivity, would also be obtained under partial oxidative conditions when the salt anion is sulfate, carbonate, or nitrate and other anions that give relatively low selectivity.
Another instance is when TMAH is used as a strong base that can also function as a phase transfer catalyst for the second embodiment. Moreover, although it has not been demonstrated for the first embodiment of the process of the invention, it is believed that partial oxidative conditions would also be effective for combinations of inorganic base and phase transfer catalyst that give low selectivity.
The oxidant used in the second and third embodiments of the invention may be the same as in the first embodiment.
The reactive contact may be carried out at a temperature of from about 20°C to about 150°C. Other conditions for the reactive contact include pressures in the range of from about 20 mbar to about 20 barg. Reaction time is typically less than about 3.5 hours. It is advantageous to agitate the reaction mixture during the entire reaction.
The reactions of step (b) of the first, second and third embodiments of the present method may be carried out in the presence of not greater than about 10:1 moles water to moles nitrobenzene. The amount of water does not include the water that hydrates with the reactants andlor with compounds formed in the process. When the mixture comprising a strong base and a phase transfer catalyst, or an organic base and inorganic salt or metal organic salt, is in aqueous solution, the reaction may be carried out with a continuous distillation of aniline-water azeotrope.
The first embodiment of the invention may be carried out with the phase transfer catalyst being tetramethylammonium bromide and the strong base comprising one or more inorganic bases.
The aqueous phase may be reused to form a new reaction mixture. Fresh base and phase transfer catalyst or organic base and inorganic salt or metal organic salt are added to replace losses by decomposition, by-product formation and solubility in the separated organic phase. Excess Aniline recovered by distillation from the reaction product mixture may be combined with make-up fresh aniline for recycle to form a new reaction mixture. Recovery of excess nitrobenzene is preferably carried out prior to hydrogenation of the 4-ADPA
intermediate by a separation step and the recovered nitrobenzene may be combined with make-up fresh nitrobenzene for use in the process, or hydrogenated to aniline.
The method of the present invention for the preparation of 4 aminodiphenylamines intermediates may be conducted as a batch process or may be performed continuously using means and equipment well known to the skilled person.
The reactive contact in step (a) in the first, second and third embodiments of the method of the invention may occur in a suitable solvent system. A
suitable solvent system comprises a polar aprotic solvent. The polar aprotic solvent may be selected form the group consisting of, but not limited to, dimethyl sulfoxide, benzyl ether, 1-Methyl-2-pyrrolidinone and N,N-dimethylformamide.
The invention, in its second embodiment, is a method where the strong base also functions as a phase transfer catalyst and the reaction may be in the absence of an alkali metal hydroxide. In that case the strong base/phase transfer catalyst is defined by formula II above.
The invention is illustrated by the following examples.
Experimental conditions are detailed within individual examples. In examples 1-10 the charging of reactors was performed in open air resulting in some free oxygen being present during the reactions, even when the reactor was stoppered, except for experiments, where indicated, run for comparative purposes. No attempt was made to remove water from the reaction mixtures in examples 1- 10.
In examples 11-16 a flow of air was supplied to the reactor headspace during all or part of charging reactants, heat-up to reaction temperature, nitrobenzene feed and hold, resulting in free oxygen being present during the reaction, except where indicated. Water was removed from the reaction mixture by azeotropic distillation with aniline. However, the reaction can also be effective without the azeotropic removal of water with aniline.
ANALYTICAL
Yields of individual components were determined by external standard HPLC. Approximately 0.6 grams of material to be analyzed is accurately weighed into a 50-mL volumetric flask and diluted with a buffer solution containing 39% v/v water, 36% v/v acetonitrile, 24% vlv methanol and 1 % vlv pH
7 buffer. The solution is injected through a 10 pL loop onto a reversed phase Zorbax ODS HPLC column (250 x 4.6 mm) using a binary gradient pumping system and the following elution gradient at a constant flow rate of 1.5 mL/minute:
Time, minutes %A %13 37.5 0 100 Eluent A is 75°l° vlv water, 15% v/v acetonitrife and 10%
v/v methanol.
20 Eluent B is 60% v/v acetonitrile and 40% v/v methanol. Detection is UV at nm.
Conversion for examples 1-10 is calculated by sum addition of known components plus any unknown peaks {assigned an arbitrary mole weight value of 25 216, aniline + nitrobenzene) as analyzed. In some instances, sum conversion is greater than 100% due to the formation of derivatives from aniline only.
Conversion for examples 11-16 is calculated based on the amount of, unreacted nitrobenzene remaining in the final coupling reaction mass.
Conversion is assumed to be 100% if no nitrobenzene is detected.
Selectivity is defined by the formula: (p-NDPA Yield + 4-NDPA
Yield)/(total yield). 4-NDPA is 4-nitrodiphenylamine and p-NDPA is 4-nitrosodiphenylamine. Total yield is the sum of the yield of all known and unknown peaks (assigned an arbitrary mole weight value of 216, aniline +
10 nitrobenzene).
In the tables: "An Recr" refers to compounds from which aniline may be easily recovered and is a sum total of traps-azobenzene and azoxybenzene;
"Others" are aniline and nitrobenzene coupling by-products e.g. phenazine, N-15 oxy-phenazine, 2-NDPA, 4-phenazo-diphenylamine and any unknowns.
EXPERIMENTAL
Experimental conditions are detailed within individual examples.
Example 1 illustrates that 4-ADPA intermediates may be formed from aniline and nitrobenzene in the presence of an inorganic base (potassium hydroxide) and phase transfer catalyst (tetramethylammonium chloride, TMACI) in a solvent-free system under relatively mild conditions. Yield of desired products is dependent on the amount of phase transfer catalyst added.
Aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99%, 4.97 grams, 40 mrfioles), potassium hydroxide (86% ground powder, 7.83 grams, 120 mmoles) and tetramethylammonium chloride were charged to a 50-mL round bottom flask equipped with magnetic stirrer in the amount indicated in Table 1 below. The reaction was allowed to proceed for 1 hour at 60°C in a stoppered flask. Contents were then sampled and analyzed by HPLC.
i Table 1 Yield, Conversionp-NDPA4-NDPA Other An Recr No TMACI added, KOH Only 26.3% 0.8 4.8 5,5 15.2 1.81 grams TMACI, 16 mmoles 59.2% 10.9 26.9 18.4 3.0 (0.4 vs NB) 3.62 grams TMACI, 32 mmoles 90.1 22.4 36.1 28.6 3.0 (0.8 vs NB) %
5.42 grams TMACI, 48 mmoles 98.2% 27.0 37.8 3.0 (1.2 vs NB) 30.3 7.23 grams TMACI, 64 mmoles g4,4% 26.5 36.2 28.9 2.9 (1.6 vs NB) 9.04 grams TMACI, 80 mmoles 98.9% 26.2 36.7 31.8 4.2 (2.0 vs NB) Similar results were obtained when running the reaction under slightly varying conditions (equimolar An/NB, higher reaction temperature, longer cycle time, water addition, etc.) as given below in Table 2.
Aniline (99%, 2.33 grams, 24.8 mmoles), nitrobenzene (99%, 3.08 grams, 24.8 mmoles), potassium hydroxide (86% ground powder, 9.77 grams, 150 mmoles), tetramethylammonium chloride (97%, see Table 2) and water (Table 2) were charged to a 50-mL round bottom flask equipped with magnetic stirrer. The water amount was 20% by weight of total reactor charge assuming 14% w/w H20 from KOH. The reaction was allowed to proceed for 2 hours at 80°C in an open flask. Contents were then sampled and analyzed by HPLC.
Table 2 Yield, Conversion p-NDPA 4-NDPA An Recr Other No TMACI, KOH Only & 2.15 g H20 2.3% 0.0 0.4 0.4 1.5 0.17 g TMACI, 1.5 mmoles (.06 vs NB) & 2.19 g H20 8.1 % 0.3 5.9 0.7 1.2 0.34 g TMACI, 3.0 mmoles (.12 vs NB) 14.7% 0.7 12.7 ' 0.3 1.0 & 2.23 g H20 0.69 g TMACI, 6.1 mmoles (.25 vs NB) 34.4% 1.7 27.7 2.9 2.1 & 2.32 g H20 1.03_g TMACI, 9.1 mmoles (.37 vs NB) 47.5% 1.6 39.5 4.2 2.2 & 2.41 g H20 1.37 g TMACI, 12.1 mmoles (.49 vs 57.8% 2.6 46.7 5.2 3.3 NB) & 2.49 g HBO
2.06 g TMACI, 18.2 mmoles (.74 vs 89.6% 7.6 61.3 17.7 3.0 NB) & 2.67 g H20 2.74 g TMACI, 24.3 mmoles (.98 vs 92.2% 11.9 64.9 13.4 2.0 NB) & 2.84 g H20 The yield of 4-ADPA intermediates was increased from < 1 % when no tetramethylammonium chloride was used to almost 77% when a near equimolar amount of phase transfer catalyst vs. nitrobenzene was added.
In both instances, more p-NDPA relative to 4-NDPA was produced as the tetramethylammonium chloride charge was increased. Also, more p-NDPA was formed in the presence of excess aniline (see Example 7).
Example 2 demonstrates that any of several phase transfer catalysts may be used with KOH to produce p-NDPA and 4-NDPA from aniline and nitrobenzene. Results are arranged in order of descending yield.
Charge to 50-mL round bottom flask equipped with magnetic stirrer:
aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99°I°, 4.97 grams, 40 mmoles), potassium hydroxide (86% ground powder, 7.83 grams, 120 mmoles) and the indicated phase transfer catalyst given in Table 3 below where the amount of phase transfer catalyst is equal to the limiting reagent charge.
(NOTE:
Some experiments run on 20 or 30 mmole scale as denoted.) Reaction was allowed to proceed for 1 hour at 60°C in a stoppered flask. Contents were then sampled and analyzed by HPLC.
Results in Table 3 above illustrate that the addition of a phase transfer catalyst improves the yield of desired products in all cases.
Tetramethylammonium chloride, fluoride, hydroxide, carbonate, formate and acetate; tetrabutyiammonium hydrogensuffate and sulfate;
methyltributylammonium chloride; and benzyltrimethylammonium hydroxide (Triton B) are most effective as phase transfer catalysts in combination with an inorganic base. Others such as tricaprylmethylammonium chloride (Aliquat 336), tetrabutylammonium chloride, tetramethylammonium nitrate, and choline hydroxide are moderately efficient. Bromide and iodide salts and the zwitterion betaine are not as suitable. Periodic trends are observed for the tetramethylammonium salts as yield, conversion and selectivity are all decreased when going down in the series from fluoride to iodide.
2.06 g TMACI, 18.2 mmoles (.74 vs 89.6% 7.6 61.3 17.7 3.0 NB) & 2.67 g H20 2.74 g TMACI, 24.3 mmoles (.98 vs 92.2% 11.9 64.9 13.4 2.0 NB) & 2.84 g H20 The yield of 4-ADPA intermediates was increased from < 1 % when no tetramethylammonium chloride was used to almost 77% when a near equimolar amount of phase transfer catalyst vs. nitrobenzene was added.
In both instances, more p-NDPA relative to 4-NDPA was produced as the tetramethylammonium chloride charge was increased. Also, more p-NDPA was formed in the presence of excess aniline (see Example 7).
Example 2 demonstrates that any of several phase transfer catalysts may be used with KOH to produce p-NDPA and 4-NDPA from aniline and nitrobenzene. Results are arranged in order of descending yield.
Charge to 50-mL round bottom flask equipped with magnetic stirrer:
aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99°I°, 4.97 grams, 40 mmoles), potassium hydroxide (86% ground powder, 7.83 grams, 120 mmoles) and the indicated phase transfer catalyst given in Table 3 below where the amount of phase transfer catalyst is equal to the limiting reagent charge.
(NOTE:
Some experiments run on 20 or 30 mmole scale as denoted.) Reaction was allowed to proceed for 1 hour at 60°C in a stoppered flask. Contents were then sampled and analyzed by HPLC.
Results in Table 3 above illustrate that the addition of a phase transfer catalyst improves the yield of desired products in all cases.
Tetramethylammonium chloride, fluoride, hydroxide, carbonate, formate and acetate; tetrabutyiammonium hydrogensuffate and sulfate;
methyltributylammonium chloride; and benzyltrimethylammonium hydroxide (Triton B) are most effective as phase transfer catalysts in combination with an inorganic base. Others such as tricaprylmethylammonium chloride (Aliquat 336), tetrabutylammonium chloride, tetramethylammonium nitrate, and choline hydroxide are moderately efficient. Bromide and iodide salts and the zwitterion betaine are not as suitable. Periodic trends are observed for the tetramethylammonium salts as yield, conversion and selectivity are all decreased when going down in the series from fluoride to iodide.
Table 3 Yield, Conversion p-NDPA Other An Recr Tetrabutylammonium sulfate, 75% 99.2% 56.1 21.2 20.1 1.8 aq., 15.49 gms~
Tetrabutylammonium hydrogensulfate,96.6% 47.9 25.0 21.2 2.4 97%, 10.50 gms*
Tetramethylammonium carbonate, 97.6% 46.6 24.6 23.7 2.8 60% aq., 6.94 gms~
Tetramethylammonium fluoride 103.6% 42.4 27.2 27.4 6.6 ~ 4 H20, 98%, 6.74 gms Tetramethylammonium acetate, 104.3% 25.9 43.1 35.0 0.4 95t, 5.61 gms Tetramethylammonium hydroxide 105.0% 38.4 29.6 30.4 6.5 ~ 5 HzO, 97%, 7.47 gms Tetramethylammonium chloride, 98.8% 24.3 37.1 30.8 6.6 97%, 4.52 gms Methyltributylammonium chloride,81.7% 23.5 30.6 22.2 5.4 75% aq., 12.58 gms Tetramethylammonium formate, 74.9% 29.0 23.8 21.0 1.1 50% aq., 9.53 gms Benzyltrimethylammonium hydroxide,52.5% 39.6 6.2 5.5 1.2 40% aq., 16.73 gms Tricaprylmethylammonium chloride,67.0% 19.1 21,3 19.6 7.0 99+%, 16.17 gms Tetramethylammonium nitrate, 61.3% 12.0 27.4 19.6 2.4 96%, 5,67 gms Choline hydroxide, 50% aq., 9.6959.0% 26.2 6.7 19.6 6.6 gms Tetrabutylammonium chloride ~ 42.6!0 8.2 23.8 9.3 1.2 H20, 98%, 8.51 gms*
Betaine, 98%, 4.78 gms 55,0% 13.0 17.2 19.6 5.2 Cetyltrimethylammonium bromide, 36.2% 7.0 19.3 8.7 1.1 95%, 11.51 gms*
Tetramethylammonium bromide, 36.5l0 11.3 12.2 6.7 6.3 98%, 6.29 gms Tetrabutylammonium bromide, 99%,34.1 8.3 14.2 5.8 5.7 13.03 gms %
Polyethylene glycol (MW = 200), 33.4% 11.9 0.6 17.2 3.7 8.00 gms Tetramethylammonium iodide, 99%,27.8% 2.4 8.0 5.8 11.6 8.12 gms Tetrabutylphosphonium bromide, 25.6% 1.6 5.1 9.4 10.0 98!0, 13.58 gms KOH Only, No phase transfer catalyst19.6% 1.2 4.0 3.3 11.0 added *30 mmofe scale (16.93 gms aniline, listed) 3.73 gms nitrobenzene, 5.87 gms KOH & PTC as ~20 mmoles (TMA)zC03 & (TBA)ZS04same (0.5 to 1 vs NB, no.
of equivalents) Example 3 shows that nitrobenzene may be coupled with a variety of aniline derivatives to produce 4-ADPA intermediates.
A stoichiometric amount of substrate as listed in Table 4 below;
5 nitrobenzene (99%, 3.08 grams, 24.8 mmoles), potassium hydroxide (86%
ground powder, 9.77 grams, 150 mmofes), tetramethylammonium chloride (97°!°, 2.74 grams, 24.3 mmoles), and water (2.84 grams) were charged to a 50-mL
round bottom flask equipped with a magnetic stirrer. The reaction was allowed to proceed for 2 hours at 80°C in an open flask. Contents were then sampled and 10 analyzed by HPLC.
Table 4 Yield, Conversion-NDPA 4-NDPA Other p An Recr Aniline, 99%, 2.33 grams, 95.4% 6.0 68.3 19.9 1.2 24.8 mmoles Formanilide, 99%, 3.03 grams,84.5% 19.3 47.3 16.3 1.5 24.8 mmoles Phenylurea, 97%, 3.40 grams, 96.2I 19.2 38.8 13.5 24.8 24.2 mmoles Carbanilide, 98%, 2.65 grams,48.1 1.3 37.1 9.3 0,4 12.2 mmoles %
Thiocarbanilide, 98%, 2.85 58.6% 5.4 31.6 18.6 3.0 grams, 12.2 mmoles Acetanilide, 97%, 3.38 grams,8.5l 0.3 2.7 3.6 1.9 24.3 mmoles Benzamide, 99%, 3.03 grams, 49.4% 0.0 1.0 15.1 33.3 24.8 mmoles N-Methyl-Benzamide, 99+1, 8.2% 0.0 0.0 0.0 8.2 3.38 grams, 25.0 mmoles Benzanilide, 98%, 2.47 grams,0.1% 0.0 0.1 0.0 0.0 12.3 mmoles While aniline most effectively couples with nitrobenzene in a KOH-TMACI
system, amides such as formanilide, phenylurea and carbanilide as well as the thiocarbanilide can be substituted to produce 4-ADPA intermediates.
Example 4 illustrates the reaction of aniline and nitrobenzene using various bases in combination with tetramethylammonium chloride to produce 4-ADPA intermediates.
Aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99%, 4.97 grams, 40 mmoles), an appropriate amount of base as given in Table 5 below and tetramethylammonium chloride (97°l0, 4.52 grams, 40 mmoles) was charged to a 50-mL round bottom flask equipped with a magnetic stirrer. The reaction was allowed to proceed for 1 hour at 60°G in a stoppered flask. Contents were then sampled and analyzed by HPLG.
Table 5 Yield, Conversion p-NDPA4-NDPA An Other Recr 97.1 KOH, 86l0, 7.83 grams, 25.2 35.5 30.6 5.8 120 mmoles (3:1 vs NB) 100.5%
KOH, 86l0, 13.05 grams, 21.5 36.0 32.0 11.0 200 mmoles (5:1 vs NB) 21.3%
NaOH, 98l0, 4.90 grams, 4.7 12.6 3.4 0.6 , 120 mmoles (3:1 vs NB) 50.4%
NaOH, 98l0, 8.16 grams, 11.5 24.5 14.2 0.2 200 mmoles (5:1 vs NB) 98.8%
CsOH~H~O, 95l0, 15.91 grams,20.5 43.2 34.5 0.6 90 mmoles (3:1 vs NB)*
107.1 t BuOK, 95%, 11.84 grams, 15.2 33.4 25.0 33.5 100 mmofes (2'/2:1 vs NB) 51.5%
TMAH~5H20, 22.42 grams, 38.2 7.0 5.9 0.4 120 mmoles (3:1 vs NB)~
*30 mmole scale (16.93 gms 3.73 gms nitrobenzene, aniline, 3.39 gms TMACI
& base as indicated) ~ Tetramethylammonium hydroxide only. No TMACI added.
Both lithium and calcium hydroxide were screened with no reaction 2p observed for either of these two bases.
Potassium hydroxide is the preferred base but sodium hydroxide, cesium hydroxide, potassium t-butoxide and tetramethylammonium hydroxide are also suitable bases any of which may used in combination with tetramethylammonium chloride to obtain acceptable rates of conversion.
Example 5 demonstrates the effect ofi increasing potassium hydroxide charge on aniline-nitrobenzene coupling products under otherwise constant reaction conditions with tetramethylammonium chloride as a phase transfer catalyst.
Aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99%, 4.97 grams, 40 mmoles), potassium hydroxide in the amount given in Table 6 below and tetramethylammonium chloride (97%, 4.52 grams, 40 mmoles) was charged to a 50-mL round bottom flask equipped with magnetic stirrer. The reaction was allowed to proceed for 1 hour at 60°C in a stoppered flask. Contents were then sampled and analyzed by HPLC.
Table 6 Yield, Conversion p-NDPA 4-NDPA An Recr Other No KOH, TMACI Only 0.0% 0.0 0.0 0.0 0.0 1.30 grams KOH, 20 mmoles (0.5;1 54,g% 18.8 19.6 15.7 0.7 vs NB) 2.61 grams KOH, 40 mmoles (1:1 69.2% 21,3 26.8 20.8 0.3 vs NB) 5.22 grams KOH, 80 mmoles (2:1 91.8% 26.0 33.5 29.1 3.2 vs NB) 7.83 grams KOH, 120 mmoles (3:1 97.1 25.2 35.5 30.6 5.8 vs NB) %
10.44 grams KOH, 160 mmoles (4:1 99.1 23.6 36.0 32.0 7.5 vs NB) %
13.05 grams KOH, 200 mmoles (5:1 100.5! 21.5 36.0 32.0 11.1 vs NB) 15.66 grams KOH, 240 mmoles (6:1 101.7% 18.4 33.6 32.7 17.0 vs NB) Higher excesses of base result ctivity in poorer reaction sele and more by-product formation. The same trend is observed when running the reaction under comparatively milder reaction conditions as described in Table 7 below.
Similarly, conversion is a function of the amount of base used.
Aniline (99%, 32.60 grams, 346.5 mmoles), nitrobenzene (99%, 6.16 grams, 49.5 mmoles), potassium hydroxide in the amount given in Table 7 below (86% ground powder, 16,31 grams, 250 mmoles) and tetramethylammonium chloride (97%, 5.48 grams, 48.5 mmoles) were charge to a 100-mL round bottom flask equipped with a Teflon paddle stirrer. The reaction was allowed to proceed for 1 hour with no application of external heat (some exotherm generated by dissolution of KOH in reaction water) in a stoppered flask. Contents were then sampled and analyzed by HPLC.
Table 7 Yield, Conversion p-NDPA 4-NDPA An Recr Other 9.77 grams 10.5% 1.3 8.6 0.0 0.6 KOH, 150 mmoles (3:1 vs NB) 13.05 grams 200 mmoles (4:1 64.6% 14.9 26.2 15.4 8.1 KOH, vs NB) 16.31 grams 250 mmoles (5:1 92.2! 21.8 33.0 27.0 10.4 KOH, vs NB) 19.57 grams 300 mmoles (6:1 100.5% 21.7 33.6 31.8 13.5 KOH, vs NB) 22.84 rams 350 mmoles (7:1 104.4% 21.3 33.6 33.5 16.0 KOH, vs NB
Example 6 indicates the effect that the introduction of an oxidant has on the conversion of aniline and nitrobenzene to p-NDPA, 4-NDPA and by-products when utilizing a potassium hydroxide ! tetramethylammonium chloride base-PTC
system.
Aniline (99%, 2.33 grams, 24.8 mmoles), nitrobenzene (99%, 3.08 grams, 24.8 mmoles), potassium hydroxide (86% ground powder, 9.77 grams, 150 mmoles), tetramethylammonium chloride (97%, 0.69 grams, 6.1 mmoles) and water (2.32 grams) were charged to a 50-mL round bottom flask equipped with a magnetic stirrer. The reaction was allowed to proceed for 2 hours at 80°C under atmospheric conditions described below. Contents were then sampled and analyzed by HPLC.
The definition of a closed system is a stoppered flask. An open system is left unstoppered and open to the atmosphere. For gas sweep experiments, a three-necked flask is substituted for a single-necked fiask, the system equipped with both a gas inlet and outlet line, and the appropriate gas swept across the reaction mass at a low flow rate.
Table 8 Yield, Conversion Selectivity p- 4- An Recr Other NDPA NDPA
Closed System 45.1 % 61.3% 1.4 26.3 15.9 1.5 Open System 34.4% 85.6% 1.7 27.7 2.9 2.1 Gas Sweep, Nitrogen94.8% 58.2% 2.4 52.8 38.3 1.3 Gas Sweep, Air 60.6% 86.8% 2.8 49.8 3.3 4.7 In cases where the reaction is left open to excess air, selectivity is markedly improved, as opposed to experiments where the amount of oxidant is limited. Formation of azobenzene is greatly increased in the latter instance.
Improvement in reaction selectivity is reinforced by experiments in Table 9, which demonstrate the effect of hydrogen peroxide addition in the reaction mixture.
Aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99%, 4.97 grams, 40 mmoles), hydrogen peroxide (50% aqueous, amount indicated in Table 9 below), water (sum total from additional water and peroxide kept constant at 2.16 grams), potassium hydroxide (86% ground powder, 7.83 grams, 120 mmoles) and tetramethylammonium chloride (97%, 4.52 grams, 40 mmoles) was charged to a 50-mL round bottom flask equipped with a magnetic stirrer. Peroxide was charged to the reaction mixture before adding KOH & TMACI with the flask quickly stoppered and then the reaction was allowed to proceed for 1 hour at 60°C. Contents were then sampled and analyzed by HPLC.
Table Yield, An Conversion p-NDPA 4-NDPARecrOther Selectivit No H~Oz & 2.16 g water 96.6% 67.9% 27.9 37.7 30.60.5 0.27 g HzOZ, 4 mmol, (0.1 90.3% 73.8% 27.3 39.4 23.00.7 vs NB) & 2.02 g water 0.54 g Hz02, 8 mmol, (0.2 86.6% 77.7% 27.3 40.0 18.31.0 vs NB) & 1.89 g water 1.09 g H202, 16 mmol, (0.486.4% 77.3% 25.5 41.3 18.31.3 vs NB) & 1.62 g water 1.63 g H202, 24 mmol, (0.686.4% 78.4% 26.9 40.9 17.61.1 vs NB) & 1.34 g water 2.18 g H202, 32 mmol, (0.879.8% 80.3% 25.6 38.4 14.31.4 vs NB) ~
& 1.07 g water 2.72 g H~O2, 40 mmol, (1.080.8% 82.0% 25.9 40.4 13.01.6 vs NB) & 0.80 water The same trend noted for opening the reaction contents to air is also seen 10 for peroxide, namely exposure to an oxidant improves selectivity. This observation is reinforced by experimental trials where excess nitrobenzene is used to act as an oxidant. (see Example 7).
15 Example 7 shows how the ratio of 4-ADPA intermediates can be controlled by adjusting the amount of aniline charged into the reaction.
Aniline (99%, amount given in Table 10), nitrobenzene (99%, 4.97 grams, 40 mmoles), potassium hydroxide (86% ground powder, 7.83 grams, 120 20 mmoles) and tetramethylammonium chloride (97%, 4.52 grams, 40 mmoles) was charged to 50-mL round bottom flask equipped with magnetic stirrer. The reaction was allowed to proceed for 1 hour at 60°C in a stoppered flask.
Contents were then sampled and analyzed by HPLC.
Table 10 Yield, Conv Ratio p-NDPA 4-NDPA An Recr Other 35.28 grams Aniline, 375 mmoles, 87.20 1.34 36.7 27.3 22.2 1.1 15:1 vs NB*
36.69 grams Aniline, 390 mmoles, 93.2% 1.31 37.1 28.4 26.3 1.4 13:1 vs NB~
36.22 grams Aniline, 385 mmoles, 94.7% 1.14 35.2 30.9 26.5 2.2 11:1 vs NB#
33.87 grams Aniline, 360 mmoles, 95.4% 0.96 32.0 33.2 27.5 2.6 9:1 vs NB
26.34 grams Aniline, 280 mmoles, 96.8% 0.75 27.1 36.0 30.3 3.5 7:1 vs NB
18.81 grams Aniline, 200 mmofes, 95.9% 0.60 23.1 38.8 31.1 2.8' 5:1 vs NB
11.29 grams Aniline, 120 mmoles, ~ 92.3% 0.37 15.7. 42.4 30.9 3.4 3:1 vs NB
3.76 rams Aniline, 40 mmoles, 1:1 vs NB 80.1% 0.14 6.1 43.8 24.7 5.5 *25 mmole scale (35.28 gms aniline, 3.11 gms nitrobenzene, 4.89 gms KOH & 2.82 gms TMACI) ~30 mmole scale (36.69 gms aniline, 3.73 gms nitrobenzene, 5.87 gms KOH & 3.39 gms TMACI) #35 mmole scale (36.22 gms aniline, 4.35 gms nitrobenzene, 6.85 gms KOH & 3.95 gms TMACI) As more aniline is charged to the reaction, more p-NDPA is formed relative to 4-NDPA. The same trend is noted under differing reaction conditions as outlined in Table 11 below.
Aniline (99%, amount given in Table 11), nitrobenzene (99%, 3.08 grams, 24.8 mmoles), potassium hydroxide (86% ground powder, 9.77 grams, 150 mmoles), tetramethylammonium chloride (97%, 0.69 grams, 6.1 mmoles) and water (Table 11, 20% wlw) were charged to a 50-mL round bottom flask equipped with a magnetic stirrer. The reaction was allowed to proceed for 2 hours at 80°C in an open flask. Contents were then sampled and analyzed by MPLC.
Table 11 Yield, Conv Ratio ,o-NDPA 4-NDPA An Recr Other 12.48 g An, 133 mmol, (5.4 vs NB) & 18.6% 0.52 5.6 10.9 1.0 1.1 4.89 g HBO
8.57 g An, 91.1 mmol, (3.7 vs NB) & 26.5% 0.37 6.5 17.7 1.4 0.8 3.90 g H20 4.66 g An, 49.6 mmol, (2 vs NB) & 28.9% 0.12 2.6 20.9 3.2 2.1 2.91 g HZO
2.33 g An, 24.8 mmol, (1 vs NB) & 34.4% 0.06 1.7 27.7 2.9 2.1 2.32 g H20 1.75 g An, 18.6 mmol, (.75 vs NB) & 42.6% 0.05 1.8 34.6 4.2 2.1 2.17 g H20 1.16 g An, 12.3 mmol, (.50 vs NB) & 56.1 % 0.02 0.8 51.7 1.1 2.5 2.02 g H20 0.58 g An, 6.2 mmol, (.25 vs NB) & 76.7% 0.01 0.9 72.9 1.1 1.8 1.88 g HZO
Yields of 4-ADPA intermediates (p-NDPA + 4-NDPA) remain relatively flat when aniline is used in excess (approx. 20°I°) but improve significantly (73.8% at 0.25 to 1 AnINB) when aniline becomes the limiting reagent as noted in Table 11.
Also, selectivity is improved (96.1% at 0.25 to 1 An/NB) when nitrobenzene is used in excess despite less overall water. As shown in Example 9, less water typically decreases selectivity in an inorganic base system. Excess nitrobenzene here acts as an oxidant, improving selectivity as shown in Example 6 with air and peroxide.
Example 8 illustrates that the reaction between aniline and nitrobenzene using potassium hydroxide as a base in conjunction with tetramethyiammonium chloride can be conducted over a wide range of temperatures.
Aniline (99%, 2.33 grams, 24.8 mmoles), nitrobenzene (99%, 3.08 grams, 24.8 mmoles), potassium hydroxide (86% ground powder, 9.77 grams, 150 mmoles), tetramethylammonium chloride (97%, 0.69 grams, 6,1 mmoles) and water (2.32 grams, 20°lo wlw) were charged to a 50-mL round bottom flask equipped with magnetic stirrer. The reaction was allowed to proceed for 2 hours at the given temperature in an open flask. Contents were then sampled and analyzed by HPLG.
Table 12 Yield, Conversion -NDPA 4-NDPA An RecrOther Reaction Temperature, g,3% 0.1 8.3 0.0 1.0 Reaction Temperature, 21.6% 0,5 19.5 0.2 1.4 Reaction Temperature, 25.2% 0,8 22.3 0.1 1.9 Reaction Temperature, 26.0% 0,6 22.8 0.4 2.2 Reaction Temperature, 34.4% 1.7 27.7 2.9 2.1 Reaction Temperature, 39,3% 2.3 27.8 7.5 1.7 Reaction Temperature, 53.8% 3.5 33.4 12.8 4.0 Reaction Temperature, 72.7% 9.1 34.0 17.3 12.4 Increasing reaction temperature results~in improved yields and conversion but reaction selectivity is lost. The amount of p-NDPA, relative to 4-NDPA, increases With inct~easing temperature.
Table 13 Yield, Selectivit -NDPA I 4-NDPA
% , l Reaction Temperature, g,3 89.0 0.01 Reaction Temperature, 20.0 92.3 0.03 Reaction Temperature, 23.1 91.8 0.04 Reaction Temperature, 23.4 90.0 0.03 Reaction Temperature, 29.4 85.6 0.06 Reaction Temperature, 30.1 78.7 0.08 Reaction Temperature, 37.0 68.7 0.11 Reaction Temperature, 43.1 59.2 0.27 Example 9 emphasizes the effect of water in the reaction of aniline and nitrobenzene with a KOH-TMACI base/phase transfer system to form 4-ADPA
intermediates.
Aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99%, 4.97 grams, 40 mmoles), potassium hydroxide (86% ground powder, 7.83 grams, 120 mmoles), tetramethylammonium chloride (97%, 4.52 grams, 40 mmoles), and water as listed in Tables 14 and 15 was charged to a 50-mL round bottom flask equipped with a magnetic stirrer. The reaction was aNowed to proceed for 1 hour at 60°C in a stoppered flask. Contents were then sampled and analyzed by HPLC.
Table 14 Yield, Conversion p-NDPA 4-NDPA An Recr Other No Water added 98.6°l0 26.4 38.5 30.4 3.3 2.16 grams H20, 120 mmoles 94.7% 28.5 37.3 28.6 0.4 (3:1 vs NB) 4.32 grams H20, 240 mmoles 67.0% 27.2 21.1 18.4 0.3 (6:1 vs NB) 6.48 grams H20, 320 mmoles 28.3!0 16.3 6.7 5.1 0.2 (9:1 vs NB) 8.64 grams H20, 480 mmoles 5.5% 4.1 1.3 0.0 0.0 (12:1 vs NB) 5 Table 15 Selectivit , % -NDPA / 4-NDPA
No Water added 65.8 0.69 3:1 H~O/NB (1 mole Water vs. KOH) 69.4 0.77 6:1 H20lNB (2 moles Water vs. KOH) 72.1 1.28 9:1 H20/NB (3 moles Water vs. KOH) 81.3 2.44 12:1 HZO/NB (4 moles Water vs. KOH) 100.0 3.08 A general improvement in selectivity and higher levels of p-NDPA relative to 4-NDPA becomes evident as the amount of water is increased.
The effect of too much water may also be noted from Example 2 and Table 3 where the effectiveness of a 60% aqueous solution of tetramethylammonium carbonate as a phase transfer catalyst is shown.
Previous unreported data obtained from a dilute 25% solution indicated practically no conversion.
Example 10 shows that the reaction may be carried out in any of several solvents.
Aniline (99%, 11.29 grams, 120 mmoles), nitrobenzene (99%, 2.49 grams, 20 mmoles), potassium hydroxide (86% ground powder, 3.91 grams, 60 mmoles), tetramethylammonium chloride (97%, 2.26 grams, 20 mmoles) and 20-mL of the appropriate solvent as represented in Table 16 was charged to a 50-mL round bottom flask equipped with a magnetic stirrer. The reaction was allowed to proceed for 1 hour at 60°C in a stoppered flask. Contents were then sampled and analyzed by HPLC.
Table 16 Yield, t Conversionp-NDPA4-NDPA An Other Recr No solvent added 97.1 % 25.2 35.5 30.6 5.8 Dimethyl sulfoxide 99.5% 34.2 37.6 26.1 1.6 Dimethyl sulfoxide, No 36.5% 10.9 15.8 6.4 3.4 phase transfer catalyst added Benzyl ether 93.7% 30.6 32.1 28.1 3.0 1-Methyl-2-pyrrolidinone 80.1% 29.3 27.3 17.9 5.6 N,N-Dimethylformamide 74.0% 27.2 27.2 19.1 0.6 p-Xylene 65.9% 8.8 10.1 44.6 2.4 Toluene 63.3% 3.0 3.7 51.1 5.5 Notable is a roughly two-thirds reduction in yield when the phase transfer catalyst is omitted (26.7% in DMSO without TMACI increasing to 71.8% with TMACI).
2p Selectivity remains relatively unchanged in polar solvents (~ 70%) but plunges significantly when non-polar hydrocarbons such as p-xylene or toluene are selected as azobenzene yields in each of these two solvents exceed 40%.
Example 11 demonstrates the reaction of aniline and nitrobenzene in combination with an aqueous solution of potassium hydroxide and tetramethyalammonium chloride by continuous distillation of the aniline-water azeotrope.
111.8 grams aniline (99°l°, 1.19 moles), 31.2 grams aqueous potassium hydroxide solution (45%, 0.250 moles) and 50.0 grams aqueous tetramethylammonium chloride solution (55%, 0.25 moles) were charged to a 500-mL flask equipped with a Teflon paddle stirrer, thermocouple, nitrobenzene feed tube and needle valve. A vacuum was pulled on the mixture to 120 mm Hg, regulating pressure by bleeding air across the reactor. Heating was begun and nitrobenzene flow was started (24.6 grams, 99%, 0.20 moles) when the desired reaction temperature of 80°C was reached. The temperature was controlled by increasing the vacuum so as to complete the NB feed in approximately one hour at a final pressure of 60 mm Hg. The pressure was held for 45 minutes at 60 mm Hg to insure completeness of reaction. The mixture was quenched with 40 mL of water. HPLC analysis: 32.1% aniline, 0% NB, 20.3% p-NDPA, 7.6% 4-NDPA, 0.50% t-azobenzene and 0.05% pheanzine. Yields based on 100%
conversion of NB: 72.6% p-NDPA, 25.3%, 4-NDPA, 1.9% t azobenzene, 0.2%, phenazine.
As shown in Table 17 below, running the identical reaction in the absence of air resulted in a 12% lower yield (97.9% vs. 85.5%) and a seven fold increase in the azobenzene level. A summary of other reactions in this series is also given in Table 17 below:
Table Yield, ConversionSelectivit-NDPA 4-NDPA
t-Azo Phenazine BASELINE:
See conditions below*100.0% 97.9% 72.6 25.3 1.9 0.2 ATMOSPHERE:
Baseline conditions 100.0% 85.5% 66.5 19.0 14.2 0.3 (Vacuum, No Air) ANILINE CHARGE:
74.5 gms Aniline, 99.5% 96.2% 56.4 39.8 2.7 0.5 0.79 moles, 4:1 vs NB
149.0 gms Aniline, 100.0% 97.9% 73.8 24.1 1.8 0.3 1.58 moles, 8:1 vs NB
TEMPERATURE
70C 100.0% 98.1 65.1 33.0 1.4 0.5 %
~90C 100.0% 97.1 71.9 25.1 2.7 0.2 %
NITROBENZENE FEED
RATE:
29 minutes 1 D0.0% 85.2% 62.7 22.5 14.4 0.4 86 minutes 99.9% 96.1 76.8 19.2 3.5 0.4 %
BASE CHARGE:
18.7 g 45% KOH, 0.1583.0l0 97.6% 63.1 17.9 1.8 0.2 mol, 0.75;1 vs NB
37.4 g 45% KOH, 0.30100.0% 96.9% 72.7 24.2 2.7 0.4 mol, 1.5:1 vs NB
ATMOSPHERE:
Vacuum, No Air 100.0% 85.5% 66.5 19.0 14.2 0.3 *6:1 Aniline/NB, NB feed NB, 80C, 49 min. time, air 1.25 atmosphere moles KOH
vs This example demonstrates the reaction of aniline and nitrobenzene in the presence of an oxidant in combination with an aqueous solution of tetramethylammonium hydroxide and various inorganic salts by continuous distillation of the aniline-water azeotrope. The TMAHlsalt combination represents an ionic mixture of a potential base recycle stream from a process comprising an inorganic base and phase transfer catalyst after reduction of the coupling reaction mass to 4-ADPA.
Charged to a 500-mL round bottom flask equipped with a Teflon paddle stirrer, thermocouple, nitrobenzene feed tube and air bleed valve were: 139.7 grams aniline (99%, 1.49 moles), 73.9 grams aqueous tetramethylammonium hydroxide solution (35.5%, 0.29 moles) and an equivalent amount of salt (vs.
base, in 15% molar excess over nitrobenzene) as listed in Table 18 below. The mixture was heated for 30 minutes at 120 mm Hg and then nitrobenzene feed (30.8 grams, 99%, 0.25 moles) was started. The system pressure was regulated by adjusting the air bleed valve throughout the duration of the reaction cycle to maintain the desired temperature of 80°C and to complete the NB charge in approximately 75 minutes at a final pressure of 72 mm Hg. The mixture was held for 30 minutes at 70 mm Hg to insure completeness of reaction and then quenched with 25 mL water. Air was bled into the reactor headspace during the entire cycle of charging reactants, heating to reaction temperature, feeding nitrobenzene and holding for reaction completion. The salts are charged in molar equivalence to nitrobenzene at Salt/NB = 1.15. For example, potassium carbonate and sodium sulfate have two equivalents of inorganic cation, so that the molar ratio is 0.575.
The results with KCI at a slightly lower mole ratio to nitrobenzene agree welt with results obtained from the use of strong base and phase transfer catalyst (KOH and TMACI), with continuous distillation of the aniline-water azeotrope.
This demonstrates that use of an inorganic salt and organic base is equivalent to use of a strong base and phase transfer catalyst. It may be noted that sodium is not as effective as potassium for completing the reaction. Nitrate and bromide are also less effective anions for reaction completion at the conditions of this example. However, it should be possible to increase conversion for these salts by modifying reaction conditions, such as increasing reaction temperature.
Most significant is the positive effect of salt addition on reaction selectivity.
Comparison of the second and third experiments in Table 18 above shows that with the addition of KCI only, azobenzene was reduced by nearly two-thirds and relatively small amounts of "Other" compounds such as 4-Phenazo-5 diphenylamine were formed. The "TMAH Only" run was also characterized by high levels of compounds such as N-methylaniline and a stench of trimethylamine, both of which are indicative of base degradation.
Table 18 Conversion Selectivity Yield, p- 4- An Other NDPA NDPA Recr Comparison: KOH + TMACI,100.0 97.9 72.6 25.3 1.9 o.z *
TMAH Only, No Salt 100.0 83.8 62.4 21.4 4.4 11.8 Added 21.44 g Potassium Chloride100.0 97.2 72.3 24.8 1.5 1.4 16.82 g Sodium Chloride62.7 97.2 15.6 45.3 0.6 1.1 19.87 g Potassium Carbonate100.0 89.1 72.8 16.3 3.8 7.1 20.42 g Sodium Sulfate100.0 85.0 63.8 21.2 4.5 10.5 24.44 g Sodium Nitrate27.8 94.3 8.3 17.9 0.9 0.6 34.22 g Potassium Bromide27.0 98.4 15.6 11.0 0.3 0.2 23.58 g Sodium Acetate80.5 96.9 56.6 21.4 1.5 1.0 19.55 g Sodium Formate71.8 97.3 46.2 23.6 1.0 1.0 24.18 g Potassium Formate89.5 96.4 64.2 22.1 2.4 0.8 39.13 g KH2P04 39.3 97.4 10.0 28.3 0.8 0.2 * Mole ratios are slightly higher: KOH/NB and TMACI/NB = 1.25 This example demonstrates the effect of the mole ratio of inorganic salt to nitrobenzene. Reaction conditions were comparable to those for Example 12, except that the mole ratio of KCI to nitrobenzene was varied. The results in Tabie 19 indicate the addition of only a small amount of inorganic salt will increase selectivity. Therefore, in situations where corrosion due to high salt level is a concern, at least a modest selectivity improvement can be obtained.
Table Mole ConversionSelectivity Yield, Ratio SaItINB % % p-NDPA 4-NDPA An RecrOther TMAH Only, 0 100.0 83.8 62.4 21.4 4.4 11.8 No Salt Added 4.66 g KCI 0.25 100.0 87.1 63.4 23.7 7.8 5.1 13.05 g 0.70 100.0 93.8 72.3 21.5 5.0 1.2 KCI
21.44 g 1.15 100.0 97.2 72.3 24.8 1.5 1.4 KCi This example demonstrates the effect of adding a non-salt compound on selectivity and conversion of nitrobenzene. Reaction conditions were comparable to those for Example 12. Betaine, i.e. (acetyl)trimethylammomnium hydroxide inner salt, is a salt formed by the acetate group with the positively charged tetraalkylammonium group. So despite the name, the compound does not actually have hydroxide associated with the tetraalkylammonium group.
However, when a strong base is added, betaine is converted to a compound that contains both an acetate salt group and a tetraalkylammonium hydroxide group.
So with TMAH, betaine is converted to a compound with a tetramethylammonium-acetate group and an (acetyl)trimethylammomnium hydroxide group. With KOH, the compound has a potassium -acetate group with the (acetyl)trimethyfammomnium hydroxide group. In the KOH case, the compound represents a metal organic salt and a organic base in one molecule.
Betaine is known in the literature to be a phase transfer compound or PTC
(Starks and Liotta, ibid), as it carries the inorganic or organic base into the organic phase.
The results in Table 20 show that betaine has only a modest effect on selectivity or conversion with TMAH. The results with betainelNB =1.15 are only equivalent to KCI/NB = 0.25. Furthermore, addition of an anion without an inorganic cation (am,monium acetate) is essentially ineffective. Therefore, the use of an inorganic salt or metal organic salt is the key to best results.
Table ConversionSelectivity Yieid, Mole Ratio% I p- 4- An Other to NB NDPA NDPA Recr TMAH Only, No 0 100.0 83.8 62.4 21.4 4.4 11.8 Salt or PTC Added 4.66 g KCI 0.25 100.0 87.1 63.4 23.7 7.8 5.1 21.44 g KCI 1.15 100.0 97.2 72.3 24.8 1.5 1.4 22.16 g Ammonium1.15 0.5 100.0 0.3 0.2 0.0 0.0 Acetate 33.68 g Betaine1.15 100.0 87.6 70.7 16.9 4.8 7.6 This example illustrates that use of partial oxidative conditions can give a significant increase of selectivity. Reaction conditions were comparable to those for Example 12, except as indicated. The results are shown in Table 21.
Reaction 1 had comparable conditions to those for Example 12 throughout. For Reaction 2, the air bleed was used only during nitrobenzene feed and was stopped when 75% of the feed was completed. For Reaction 3, the nitrobenzene feed time was shortened to 45 minutes and the hold time was increased to 60 minutes, while the air bleed was used only during the nitrobenzene feed time.
It is expected that higher selectivity will also be attained for sulfate, carbonate and nitrate by use of partial oxidative conditions.
Table 21 ConversionSelectivity Yield, p-NDPA 4-NDPA An Recr Other 16.70 g KF-199.9 84.8 67.3 17.4 4.2 11.0 16.70 g KF-2100.0 91.1 80.1 11.0 6.3 2.6 16.70 g KF-3100.0 93.8 83.2 10.6 4.3 1.9 This example shows that use of an oxidant with a strong base, which also functions as a phase transfer catalyst, can increase selectivity. The reactions were done with azeotropic removal of water and aniline.
Charged to a 500-mL round bottom flask equipped with a Teflon paddle stirrer, thermocouple, nitrobenzene feed tube and air bleed valve were: 145.28 grams aniline (1.56 moles) and 87.36 grams aqueous tetramethylammonium hydroxide solution (36.0%, 0.345 moles) for Runs 1 - 3. The mixture was heated for 30 minutes at 120 mm Hg and then nitrobenzene feed (36.93 grams, 0.30 moles) was started. The system pressure was held constant at 70 mm Hg throughout the reaction period. Temperature rose from about 66°C to about 80°C during the reaction period. Nitrobenzene was charged over about 80 minutes, after which the batch was held for 40 minutes at 70 mm Hg to insure completeness of reaction and then quenched with 25 mL water. Hydrogen peroxide was charged as 20.40 grams (0.03 moles) of a 5 wt.% aqueous solution concurrently with nitrobenzene. Since water can also affect selectivity, by protecting TMAH from degradation and shifting reaction equilibria, a control was run with 20.40 grams of water that was also fed concurrently with nitrobenzene.
Runs 4 - 7 had slightly different conditions. The main difference was starting with 25 wt.% TMAH with removal of water and some aniline in the reactor prior to the nitrobenzene feed. Air was added either during the entire nitrobenzene feed or for half of the feed time.
The results in Table 22 show that hydrogen peroxide gives a larger selectivity improvement than water alone, showing that use of an oxidant can be beneficial. The results also show that addition of air as oxidant over the entire reactor cycle has a deleterious effect on selectivity. However, a selectivity improvement is obtained when the air addition is limited to part of the reaction cycle, showing that partial oxidative conditions can be beneficial. These reactions were run somewhat wetter than the case for 100%
air in Table 18, which explains the lower selectivity in Table 18. Runs 4 and 5 show the excellent repeatability of the reactions, so that selectivity increases of 1 - 2% are significant.
Table 22 Conversion Selectivity Yield, TMAH as base/PTC % % p-NDPA 4-NDPA An Recr Other 1. No oxidant 100.0 93.3 86.3 7.0 4.6 2.1 2. Water only 100.0 94.9 89.3 5.5 3.4 1,8 3. Hydrogen Peroxide 100.0 96.1 89.7 6.4 1.9 2.0 4. No oxidant 100.0 92.3 86.5 5.8 5.9 1.8 5. No oxidant 100.0 92.2 86.2 6.0 6.1 1.7 6. Air, 100% NB Feed 99.7 89.4 79.0 10.1 7.4 3.2 7. Air, 50% NB Feed 100.0 94.5 88.4 6.2 4.2 1.3
Tetrabutylammonium hydrogensulfate,96.6% 47.9 25.0 21.2 2.4 97%, 10.50 gms*
Tetramethylammonium carbonate, 97.6% 46.6 24.6 23.7 2.8 60% aq., 6.94 gms~
Tetramethylammonium fluoride 103.6% 42.4 27.2 27.4 6.6 ~ 4 H20, 98%, 6.74 gms Tetramethylammonium acetate, 104.3% 25.9 43.1 35.0 0.4 95t, 5.61 gms Tetramethylammonium hydroxide 105.0% 38.4 29.6 30.4 6.5 ~ 5 HzO, 97%, 7.47 gms Tetramethylammonium chloride, 98.8% 24.3 37.1 30.8 6.6 97%, 4.52 gms Methyltributylammonium chloride,81.7% 23.5 30.6 22.2 5.4 75% aq., 12.58 gms Tetramethylammonium formate, 74.9% 29.0 23.8 21.0 1.1 50% aq., 9.53 gms Benzyltrimethylammonium hydroxide,52.5% 39.6 6.2 5.5 1.2 40% aq., 16.73 gms Tricaprylmethylammonium chloride,67.0% 19.1 21,3 19.6 7.0 99+%, 16.17 gms Tetramethylammonium nitrate, 61.3% 12.0 27.4 19.6 2.4 96%, 5,67 gms Choline hydroxide, 50% aq., 9.6959.0% 26.2 6.7 19.6 6.6 gms Tetrabutylammonium chloride ~ 42.6!0 8.2 23.8 9.3 1.2 H20, 98%, 8.51 gms*
Betaine, 98%, 4.78 gms 55,0% 13.0 17.2 19.6 5.2 Cetyltrimethylammonium bromide, 36.2% 7.0 19.3 8.7 1.1 95%, 11.51 gms*
Tetramethylammonium bromide, 36.5l0 11.3 12.2 6.7 6.3 98%, 6.29 gms Tetrabutylammonium bromide, 99%,34.1 8.3 14.2 5.8 5.7 13.03 gms %
Polyethylene glycol (MW = 200), 33.4% 11.9 0.6 17.2 3.7 8.00 gms Tetramethylammonium iodide, 99%,27.8% 2.4 8.0 5.8 11.6 8.12 gms Tetrabutylphosphonium bromide, 25.6% 1.6 5.1 9.4 10.0 98!0, 13.58 gms KOH Only, No phase transfer catalyst19.6% 1.2 4.0 3.3 11.0 added *30 mmofe scale (16.93 gms aniline, listed) 3.73 gms nitrobenzene, 5.87 gms KOH & PTC as ~20 mmoles (TMA)zC03 & (TBA)ZS04same (0.5 to 1 vs NB, no.
of equivalents) Example 3 shows that nitrobenzene may be coupled with a variety of aniline derivatives to produce 4-ADPA intermediates.
A stoichiometric amount of substrate as listed in Table 4 below;
5 nitrobenzene (99%, 3.08 grams, 24.8 mmoles), potassium hydroxide (86%
ground powder, 9.77 grams, 150 mmofes), tetramethylammonium chloride (97°!°, 2.74 grams, 24.3 mmoles), and water (2.84 grams) were charged to a 50-mL
round bottom flask equipped with a magnetic stirrer. The reaction was allowed to proceed for 2 hours at 80°C in an open flask. Contents were then sampled and 10 analyzed by HPLC.
Table 4 Yield, Conversion-NDPA 4-NDPA Other p An Recr Aniline, 99%, 2.33 grams, 95.4% 6.0 68.3 19.9 1.2 24.8 mmoles Formanilide, 99%, 3.03 grams,84.5% 19.3 47.3 16.3 1.5 24.8 mmoles Phenylurea, 97%, 3.40 grams, 96.2I 19.2 38.8 13.5 24.8 24.2 mmoles Carbanilide, 98%, 2.65 grams,48.1 1.3 37.1 9.3 0,4 12.2 mmoles %
Thiocarbanilide, 98%, 2.85 58.6% 5.4 31.6 18.6 3.0 grams, 12.2 mmoles Acetanilide, 97%, 3.38 grams,8.5l 0.3 2.7 3.6 1.9 24.3 mmoles Benzamide, 99%, 3.03 grams, 49.4% 0.0 1.0 15.1 33.3 24.8 mmoles N-Methyl-Benzamide, 99+1, 8.2% 0.0 0.0 0.0 8.2 3.38 grams, 25.0 mmoles Benzanilide, 98%, 2.47 grams,0.1% 0.0 0.1 0.0 0.0 12.3 mmoles While aniline most effectively couples with nitrobenzene in a KOH-TMACI
system, amides such as formanilide, phenylurea and carbanilide as well as the thiocarbanilide can be substituted to produce 4-ADPA intermediates.
Example 4 illustrates the reaction of aniline and nitrobenzene using various bases in combination with tetramethylammonium chloride to produce 4-ADPA intermediates.
Aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99%, 4.97 grams, 40 mmoles), an appropriate amount of base as given in Table 5 below and tetramethylammonium chloride (97°l0, 4.52 grams, 40 mmoles) was charged to a 50-mL round bottom flask equipped with a magnetic stirrer. The reaction was allowed to proceed for 1 hour at 60°G in a stoppered flask. Contents were then sampled and analyzed by HPLG.
Table 5 Yield, Conversion p-NDPA4-NDPA An Other Recr 97.1 KOH, 86l0, 7.83 grams, 25.2 35.5 30.6 5.8 120 mmoles (3:1 vs NB) 100.5%
KOH, 86l0, 13.05 grams, 21.5 36.0 32.0 11.0 200 mmoles (5:1 vs NB) 21.3%
NaOH, 98l0, 4.90 grams, 4.7 12.6 3.4 0.6 , 120 mmoles (3:1 vs NB) 50.4%
NaOH, 98l0, 8.16 grams, 11.5 24.5 14.2 0.2 200 mmoles (5:1 vs NB) 98.8%
CsOH~H~O, 95l0, 15.91 grams,20.5 43.2 34.5 0.6 90 mmoles (3:1 vs NB)*
107.1 t BuOK, 95%, 11.84 grams, 15.2 33.4 25.0 33.5 100 mmofes (2'/2:1 vs NB) 51.5%
TMAH~5H20, 22.42 grams, 38.2 7.0 5.9 0.4 120 mmoles (3:1 vs NB)~
*30 mmole scale (16.93 gms 3.73 gms nitrobenzene, aniline, 3.39 gms TMACI
& base as indicated) ~ Tetramethylammonium hydroxide only. No TMACI added.
Both lithium and calcium hydroxide were screened with no reaction 2p observed for either of these two bases.
Potassium hydroxide is the preferred base but sodium hydroxide, cesium hydroxide, potassium t-butoxide and tetramethylammonium hydroxide are also suitable bases any of which may used in combination with tetramethylammonium chloride to obtain acceptable rates of conversion.
Example 5 demonstrates the effect ofi increasing potassium hydroxide charge on aniline-nitrobenzene coupling products under otherwise constant reaction conditions with tetramethylammonium chloride as a phase transfer catalyst.
Aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99%, 4.97 grams, 40 mmoles), potassium hydroxide in the amount given in Table 6 below and tetramethylammonium chloride (97%, 4.52 grams, 40 mmoles) was charged to a 50-mL round bottom flask equipped with magnetic stirrer. The reaction was allowed to proceed for 1 hour at 60°C in a stoppered flask. Contents were then sampled and analyzed by HPLC.
Table 6 Yield, Conversion p-NDPA 4-NDPA An Recr Other No KOH, TMACI Only 0.0% 0.0 0.0 0.0 0.0 1.30 grams KOH, 20 mmoles (0.5;1 54,g% 18.8 19.6 15.7 0.7 vs NB) 2.61 grams KOH, 40 mmoles (1:1 69.2% 21,3 26.8 20.8 0.3 vs NB) 5.22 grams KOH, 80 mmoles (2:1 91.8% 26.0 33.5 29.1 3.2 vs NB) 7.83 grams KOH, 120 mmoles (3:1 97.1 25.2 35.5 30.6 5.8 vs NB) %
10.44 grams KOH, 160 mmoles (4:1 99.1 23.6 36.0 32.0 7.5 vs NB) %
13.05 grams KOH, 200 mmoles (5:1 100.5! 21.5 36.0 32.0 11.1 vs NB) 15.66 grams KOH, 240 mmoles (6:1 101.7% 18.4 33.6 32.7 17.0 vs NB) Higher excesses of base result ctivity in poorer reaction sele and more by-product formation. The same trend is observed when running the reaction under comparatively milder reaction conditions as described in Table 7 below.
Similarly, conversion is a function of the amount of base used.
Aniline (99%, 32.60 grams, 346.5 mmoles), nitrobenzene (99%, 6.16 grams, 49.5 mmoles), potassium hydroxide in the amount given in Table 7 below (86% ground powder, 16,31 grams, 250 mmoles) and tetramethylammonium chloride (97%, 5.48 grams, 48.5 mmoles) were charge to a 100-mL round bottom flask equipped with a Teflon paddle stirrer. The reaction was allowed to proceed for 1 hour with no application of external heat (some exotherm generated by dissolution of KOH in reaction water) in a stoppered flask. Contents were then sampled and analyzed by HPLC.
Table 7 Yield, Conversion p-NDPA 4-NDPA An Recr Other 9.77 grams 10.5% 1.3 8.6 0.0 0.6 KOH, 150 mmoles (3:1 vs NB) 13.05 grams 200 mmoles (4:1 64.6% 14.9 26.2 15.4 8.1 KOH, vs NB) 16.31 grams 250 mmoles (5:1 92.2! 21.8 33.0 27.0 10.4 KOH, vs NB) 19.57 grams 300 mmoles (6:1 100.5% 21.7 33.6 31.8 13.5 KOH, vs NB) 22.84 rams 350 mmoles (7:1 104.4% 21.3 33.6 33.5 16.0 KOH, vs NB
Example 6 indicates the effect that the introduction of an oxidant has on the conversion of aniline and nitrobenzene to p-NDPA, 4-NDPA and by-products when utilizing a potassium hydroxide ! tetramethylammonium chloride base-PTC
system.
Aniline (99%, 2.33 grams, 24.8 mmoles), nitrobenzene (99%, 3.08 grams, 24.8 mmoles), potassium hydroxide (86% ground powder, 9.77 grams, 150 mmoles), tetramethylammonium chloride (97%, 0.69 grams, 6.1 mmoles) and water (2.32 grams) were charged to a 50-mL round bottom flask equipped with a magnetic stirrer. The reaction was allowed to proceed for 2 hours at 80°C under atmospheric conditions described below. Contents were then sampled and analyzed by HPLC.
The definition of a closed system is a stoppered flask. An open system is left unstoppered and open to the atmosphere. For gas sweep experiments, a three-necked flask is substituted for a single-necked fiask, the system equipped with both a gas inlet and outlet line, and the appropriate gas swept across the reaction mass at a low flow rate.
Table 8 Yield, Conversion Selectivity p- 4- An Recr Other NDPA NDPA
Closed System 45.1 % 61.3% 1.4 26.3 15.9 1.5 Open System 34.4% 85.6% 1.7 27.7 2.9 2.1 Gas Sweep, Nitrogen94.8% 58.2% 2.4 52.8 38.3 1.3 Gas Sweep, Air 60.6% 86.8% 2.8 49.8 3.3 4.7 In cases where the reaction is left open to excess air, selectivity is markedly improved, as opposed to experiments where the amount of oxidant is limited. Formation of azobenzene is greatly increased in the latter instance.
Improvement in reaction selectivity is reinforced by experiments in Table 9, which demonstrate the effect of hydrogen peroxide addition in the reaction mixture.
Aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99%, 4.97 grams, 40 mmoles), hydrogen peroxide (50% aqueous, amount indicated in Table 9 below), water (sum total from additional water and peroxide kept constant at 2.16 grams), potassium hydroxide (86% ground powder, 7.83 grams, 120 mmoles) and tetramethylammonium chloride (97%, 4.52 grams, 40 mmoles) was charged to a 50-mL round bottom flask equipped with a magnetic stirrer. Peroxide was charged to the reaction mixture before adding KOH & TMACI with the flask quickly stoppered and then the reaction was allowed to proceed for 1 hour at 60°C. Contents were then sampled and analyzed by HPLC.
Table Yield, An Conversion p-NDPA 4-NDPARecrOther Selectivit No H~Oz & 2.16 g water 96.6% 67.9% 27.9 37.7 30.60.5 0.27 g HzOZ, 4 mmol, (0.1 90.3% 73.8% 27.3 39.4 23.00.7 vs NB) & 2.02 g water 0.54 g Hz02, 8 mmol, (0.2 86.6% 77.7% 27.3 40.0 18.31.0 vs NB) & 1.89 g water 1.09 g H202, 16 mmol, (0.486.4% 77.3% 25.5 41.3 18.31.3 vs NB) & 1.62 g water 1.63 g H202, 24 mmol, (0.686.4% 78.4% 26.9 40.9 17.61.1 vs NB) & 1.34 g water 2.18 g H202, 32 mmol, (0.879.8% 80.3% 25.6 38.4 14.31.4 vs NB) ~
& 1.07 g water 2.72 g H~O2, 40 mmol, (1.080.8% 82.0% 25.9 40.4 13.01.6 vs NB) & 0.80 water The same trend noted for opening the reaction contents to air is also seen 10 for peroxide, namely exposure to an oxidant improves selectivity. This observation is reinforced by experimental trials where excess nitrobenzene is used to act as an oxidant. (see Example 7).
15 Example 7 shows how the ratio of 4-ADPA intermediates can be controlled by adjusting the amount of aniline charged into the reaction.
Aniline (99%, amount given in Table 10), nitrobenzene (99%, 4.97 grams, 40 mmoles), potassium hydroxide (86% ground powder, 7.83 grams, 120 20 mmoles) and tetramethylammonium chloride (97%, 4.52 grams, 40 mmoles) was charged to 50-mL round bottom flask equipped with magnetic stirrer. The reaction was allowed to proceed for 1 hour at 60°C in a stoppered flask.
Contents were then sampled and analyzed by HPLC.
Table 10 Yield, Conv Ratio p-NDPA 4-NDPA An Recr Other 35.28 grams Aniline, 375 mmoles, 87.20 1.34 36.7 27.3 22.2 1.1 15:1 vs NB*
36.69 grams Aniline, 390 mmoles, 93.2% 1.31 37.1 28.4 26.3 1.4 13:1 vs NB~
36.22 grams Aniline, 385 mmoles, 94.7% 1.14 35.2 30.9 26.5 2.2 11:1 vs NB#
33.87 grams Aniline, 360 mmoles, 95.4% 0.96 32.0 33.2 27.5 2.6 9:1 vs NB
26.34 grams Aniline, 280 mmoles, 96.8% 0.75 27.1 36.0 30.3 3.5 7:1 vs NB
18.81 grams Aniline, 200 mmofes, 95.9% 0.60 23.1 38.8 31.1 2.8' 5:1 vs NB
11.29 grams Aniline, 120 mmoles, ~ 92.3% 0.37 15.7. 42.4 30.9 3.4 3:1 vs NB
3.76 rams Aniline, 40 mmoles, 1:1 vs NB 80.1% 0.14 6.1 43.8 24.7 5.5 *25 mmole scale (35.28 gms aniline, 3.11 gms nitrobenzene, 4.89 gms KOH & 2.82 gms TMACI) ~30 mmole scale (36.69 gms aniline, 3.73 gms nitrobenzene, 5.87 gms KOH & 3.39 gms TMACI) #35 mmole scale (36.22 gms aniline, 4.35 gms nitrobenzene, 6.85 gms KOH & 3.95 gms TMACI) As more aniline is charged to the reaction, more p-NDPA is formed relative to 4-NDPA. The same trend is noted under differing reaction conditions as outlined in Table 11 below.
Aniline (99%, amount given in Table 11), nitrobenzene (99%, 3.08 grams, 24.8 mmoles), potassium hydroxide (86% ground powder, 9.77 grams, 150 mmoles), tetramethylammonium chloride (97%, 0.69 grams, 6.1 mmoles) and water (Table 11, 20% wlw) were charged to a 50-mL round bottom flask equipped with a magnetic stirrer. The reaction was allowed to proceed for 2 hours at 80°C in an open flask. Contents were then sampled and analyzed by MPLC.
Table 11 Yield, Conv Ratio ,o-NDPA 4-NDPA An Recr Other 12.48 g An, 133 mmol, (5.4 vs NB) & 18.6% 0.52 5.6 10.9 1.0 1.1 4.89 g HBO
8.57 g An, 91.1 mmol, (3.7 vs NB) & 26.5% 0.37 6.5 17.7 1.4 0.8 3.90 g H20 4.66 g An, 49.6 mmol, (2 vs NB) & 28.9% 0.12 2.6 20.9 3.2 2.1 2.91 g HZO
2.33 g An, 24.8 mmol, (1 vs NB) & 34.4% 0.06 1.7 27.7 2.9 2.1 2.32 g H20 1.75 g An, 18.6 mmol, (.75 vs NB) & 42.6% 0.05 1.8 34.6 4.2 2.1 2.17 g H20 1.16 g An, 12.3 mmol, (.50 vs NB) & 56.1 % 0.02 0.8 51.7 1.1 2.5 2.02 g H20 0.58 g An, 6.2 mmol, (.25 vs NB) & 76.7% 0.01 0.9 72.9 1.1 1.8 1.88 g HZO
Yields of 4-ADPA intermediates (p-NDPA + 4-NDPA) remain relatively flat when aniline is used in excess (approx. 20°I°) but improve significantly (73.8% at 0.25 to 1 AnINB) when aniline becomes the limiting reagent as noted in Table 11.
Also, selectivity is improved (96.1% at 0.25 to 1 An/NB) when nitrobenzene is used in excess despite less overall water. As shown in Example 9, less water typically decreases selectivity in an inorganic base system. Excess nitrobenzene here acts as an oxidant, improving selectivity as shown in Example 6 with air and peroxide.
Example 8 illustrates that the reaction between aniline and nitrobenzene using potassium hydroxide as a base in conjunction with tetramethyiammonium chloride can be conducted over a wide range of temperatures.
Aniline (99%, 2.33 grams, 24.8 mmoles), nitrobenzene (99%, 3.08 grams, 24.8 mmoles), potassium hydroxide (86% ground powder, 9.77 grams, 150 mmoles), tetramethylammonium chloride (97%, 0.69 grams, 6,1 mmoles) and water (2.32 grams, 20°lo wlw) were charged to a 50-mL round bottom flask equipped with magnetic stirrer. The reaction was allowed to proceed for 2 hours at the given temperature in an open flask. Contents were then sampled and analyzed by HPLG.
Table 12 Yield, Conversion -NDPA 4-NDPA An RecrOther Reaction Temperature, g,3% 0.1 8.3 0.0 1.0 Reaction Temperature, 21.6% 0,5 19.5 0.2 1.4 Reaction Temperature, 25.2% 0,8 22.3 0.1 1.9 Reaction Temperature, 26.0% 0,6 22.8 0.4 2.2 Reaction Temperature, 34.4% 1.7 27.7 2.9 2.1 Reaction Temperature, 39,3% 2.3 27.8 7.5 1.7 Reaction Temperature, 53.8% 3.5 33.4 12.8 4.0 Reaction Temperature, 72.7% 9.1 34.0 17.3 12.4 Increasing reaction temperature results~in improved yields and conversion but reaction selectivity is lost. The amount of p-NDPA, relative to 4-NDPA, increases With inct~easing temperature.
Table 13 Yield, Selectivit -NDPA I 4-NDPA
% , l Reaction Temperature, g,3 89.0 0.01 Reaction Temperature, 20.0 92.3 0.03 Reaction Temperature, 23.1 91.8 0.04 Reaction Temperature, 23.4 90.0 0.03 Reaction Temperature, 29.4 85.6 0.06 Reaction Temperature, 30.1 78.7 0.08 Reaction Temperature, 37.0 68.7 0.11 Reaction Temperature, 43.1 59.2 0.27 Example 9 emphasizes the effect of water in the reaction of aniline and nitrobenzene with a KOH-TMACI base/phase transfer system to form 4-ADPA
intermediates.
Aniline (99%, 22.58 grams, 240 mmoles), nitrobenzene (99%, 4.97 grams, 40 mmoles), potassium hydroxide (86% ground powder, 7.83 grams, 120 mmoles), tetramethylammonium chloride (97%, 4.52 grams, 40 mmoles), and water as listed in Tables 14 and 15 was charged to a 50-mL round bottom flask equipped with a magnetic stirrer. The reaction was aNowed to proceed for 1 hour at 60°C in a stoppered flask. Contents were then sampled and analyzed by HPLC.
Table 14 Yield, Conversion p-NDPA 4-NDPA An Recr Other No Water added 98.6°l0 26.4 38.5 30.4 3.3 2.16 grams H20, 120 mmoles 94.7% 28.5 37.3 28.6 0.4 (3:1 vs NB) 4.32 grams H20, 240 mmoles 67.0% 27.2 21.1 18.4 0.3 (6:1 vs NB) 6.48 grams H20, 320 mmoles 28.3!0 16.3 6.7 5.1 0.2 (9:1 vs NB) 8.64 grams H20, 480 mmoles 5.5% 4.1 1.3 0.0 0.0 (12:1 vs NB) 5 Table 15 Selectivit , % -NDPA / 4-NDPA
No Water added 65.8 0.69 3:1 H~O/NB (1 mole Water vs. KOH) 69.4 0.77 6:1 H20lNB (2 moles Water vs. KOH) 72.1 1.28 9:1 H20/NB (3 moles Water vs. KOH) 81.3 2.44 12:1 HZO/NB (4 moles Water vs. KOH) 100.0 3.08 A general improvement in selectivity and higher levels of p-NDPA relative to 4-NDPA becomes evident as the amount of water is increased.
The effect of too much water may also be noted from Example 2 and Table 3 where the effectiveness of a 60% aqueous solution of tetramethylammonium carbonate as a phase transfer catalyst is shown.
Previous unreported data obtained from a dilute 25% solution indicated practically no conversion.
Example 10 shows that the reaction may be carried out in any of several solvents.
Aniline (99%, 11.29 grams, 120 mmoles), nitrobenzene (99%, 2.49 grams, 20 mmoles), potassium hydroxide (86% ground powder, 3.91 grams, 60 mmoles), tetramethylammonium chloride (97%, 2.26 grams, 20 mmoles) and 20-mL of the appropriate solvent as represented in Table 16 was charged to a 50-mL round bottom flask equipped with a magnetic stirrer. The reaction was allowed to proceed for 1 hour at 60°C in a stoppered flask. Contents were then sampled and analyzed by HPLC.
Table 16 Yield, t Conversionp-NDPA4-NDPA An Other Recr No solvent added 97.1 % 25.2 35.5 30.6 5.8 Dimethyl sulfoxide 99.5% 34.2 37.6 26.1 1.6 Dimethyl sulfoxide, No 36.5% 10.9 15.8 6.4 3.4 phase transfer catalyst added Benzyl ether 93.7% 30.6 32.1 28.1 3.0 1-Methyl-2-pyrrolidinone 80.1% 29.3 27.3 17.9 5.6 N,N-Dimethylformamide 74.0% 27.2 27.2 19.1 0.6 p-Xylene 65.9% 8.8 10.1 44.6 2.4 Toluene 63.3% 3.0 3.7 51.1 5.5 Notable is a roughly two-thirds reduction in yield when the phase transfer catalyst is omitted (26.7% in DMSO without TMACI increasing to 71.8% with TMACI).
2p Selectivity remains relatively unchanged in polar solvents (~ 70%) but plunges significantly when non-polar hydrocarbons such as p-xylene or toluene are selected as azobenzene yields in each of these two solvents exceed 40%.
Example 11 demonstrates the reaction of aniline and nitrobenzene in combination with an aqueous solution of potassium hydroxide and tetramethyalammonium chloride by continuous distillation of the aniline-water azeotrope.
111.8 grams aniline (99°l°, 1.19 moles), 31.2 grams aqueous potassium hydroxide solution (45%, 0.250 moles) and 50.0 grams aqueous tetramethylammonium chloride solution (55%, 0.25 moles) were charged to a 500-mL flask equipped with a Teflon paddle stirrer, thermocouple, nitrobenzene feed tube and needle valve. A vacuum was pulled on the mixture to 120 mm Hg, regulating pressure by bleeding air across the reactor. Heating was begun and nitrobenzene flow was started (24.6 grams, 99%, 0.20 moles) when the desired reaction temperature of 80°C was reached. The temperature was controlled by increasing the vacuum so as to complete the NB feed in approximately one hour at a final pressure of 60 mm Hg. The pressure was held for 45 minutes at 60 mm Hg to insure completeness of reaction. The mixture was quenched with 40 mL of water. HPLC analysis: 32.1% aniline, 0% NB, 20.3% p-NDPA, 7.6% 4-NDPA, 0.50% t-azobenzene and 0.05% pheanzine. Yields based on 100%
conversion of NB: 72.6% p-NDPA, 25.3%, 4-NDPA, 1.9% t azobenzene, 0.2%, phenazine.
As shown in Table 17 below, running the identical reaction in the absence of air resulted in a 12% lower yield (97.9% vs. 85.5%) and a seven fold increase in the azobenzene level. A summary of other reactions in this series is also given in Table 17 below:
Table Yield, ConversionSelectivit-NDPA 4-NDPA
t-Azo Phenazine BASELINE:
See conditions below*100.0% 97.9% 72.6 25.3 1.9 0.2 ATMOSPHERE:
Baseline conditions 100.0% 85.5% 66.5 19.0 14.2 0.3 (Vacuum, No Air) ANILINE CHARGE:
74.5 gms Aniline, 99.5% 96.2% 56.4 39.8 2.7 0.5 0.79 moles, 4:1 vs NB
149.0 gms Aniline, 100.0% 97.9% 73.8 24.1 1.8 0.3 1.58 moles, 8:1 vs NB
TEMPERATURE
70C 100.0% 98.1 65.1 33.0 1.4 0.5 %
~90C 100.0% 97.1 71.9 25.1 2.7 0.2 %
NITROBENZENE FEED
RATE:
29 minutes 1 D0.0% 85.2% 62.7 22.5 14.4 0.4 86 minutes 99.9% 96.1 76.8 19.2 3.5 0.4 %
BASE CHARGE:
18.7 g 45% KOH, 0.1583.0l0 97.6% 63.1 17.9 1.8 0.2 mol, 0.75;1 vs NB
37.4 g 45% KOH, 0.30100.0% 96.9% 72.7 24.2 2.7 0.4 mol, 1.5:1 vs NB
ATMOSPHERE:
Vacuum, No Air 100.0% 85.5% 66.5 19.0 14.2 0.3 *6:1 Aniline/NB, NB feed NB, 80C, 49 min. time, air 1.25 atmosphere moles KOH
vs This example demonstrates the reaction of aniline and nitrobenzene in the presence of an oxidant in combination with an aqueous solution of tetramethylammonium hydroxide and various inorganic salts by continuous distillation of the aniline-water azeotrope. The TMAHlsalt combination represents an ionic mixture of a potential base recycle stream from a process comprising an inorganic base and phase transfer catalyst after reduction of the coupling reaction mass to 4-ADPA.
Charged to a 500-mL round bottom flask equipped with a Teflon paddle stirrer, thermocouple, nitrobenzene feed tube and air bleed valve were: 139.7 grams aniline (99%, 1.49 moles), 73.9 grams aqueous tetramethylammonium hydroxide solution (35.5%, 0.29 moles) and an equivalent amount of salt (vs.
base, in 15% molar excess over nitrobenzene) as listed in Table 18 below. The mixture was heated for 30 minutes at 120 mm Hg and then nitrobenzene feed (30.8 grams, 99%, 0.25 moles) was started. The system pressure was regulated by adjusting the air bleed valve throughout the duration of the reaction cycle to maintain the desired temperature of 80°C and to complete the NB charge in approximately 75 minutes at a final pressure of 72 mm Hg. The mixture was held for 30 minutes at 70 mm Hg to insure completeness of reaction and then quenched with 25 mL water. Air was bled into the reactor headspace during the entire cycle of charging reactants, heating to reaction temperature, feeding nitrobenzene and holding for reaction completion. The salts are charged in molar equivalence to nitrobenzene at Salt/NB = 1.15. For example, potassium carbonate and sodium sulfate have two equivalents of inorganic cation, so that the molar ratio is 0.575.
The results with KCI at a slightly lower mole ratio to nitrobenzene agree welt with results obtained from the use of strong base and phase transfer catalyst (KOH and TMACI), with continuous distillation of the aniline-water azeotrope.
This demonstrates that use of an inorganic salt and organic base is equivalent to use of a strong base and phase transfer catalyst. It may be noted that sodium is not as effective as potassium for completing the reaction. Nitrate and bromide are also less effective anions for reaction completion at the conditions of this example. However, it should be possible to increase conversion for these salts by modifying reaction conditions, such as increasing reaction temperature.
Most significant is the positive effect of salt addition on reaction selectivity.
Comparison of the second and third experiments in Table 18 above shows that with the addition of KCI only, azobenzene was reduced by nearly two-thirds and relatively small amounts of "Other" compounds such as 4-Phenazo-5 diphenylamine were formed. The "TMAH Only" run was also characterized by high levels of compounds such as N-methylaniline and a stench of trimethylamine, both of which are indicative of base degradation.
Table 18 Conversion Selectivity Yield, p- 4- An Other NDPA NDPA Recr Comparison: KOH + TMACI,100.0 97.9 72.6 25.3 1.9 o.z *
TMAH Only, No Salt 100.0 83.8 62.4 21.4 4.4 11.8 Added 21.44 g Potassium Chloride100.0 97.2 72.3 24.8 1.5 1.4 16.82 g Sodium Chloride62.7 97.2 15.6 45.3 0.6 1.1 19.87 g Potassium Carbonate100.0 89.1 72.8 16.3 3.8 7.1 20.42 g Sodium Sulfate100.0 85.0 63.8 21.2 4.5 10.5 24.44 g Sodium Nitrate27.8 94.3 8.3 17.9 0.9 0.6 34.22 g Potassium Bromide27.0 98.4 15.6 11.0 0.3 0.2 23.58 g Sodium Acetate80.5 96.9 56.6 21.4 1.5 1.0 19.55 g Sodium Formate71.8 97.3 46.2 23.6 1.0 1.0 24.18 g Potassium Formate89.5 96.4 64.2 22.1 2.4 0.8 39.13 g KH2P04 39.3 97.4 10.0 28.3 0.8 0.2 * Mole ratios are slightly higher: KOH/NB and TMACI/NB = 1.25 This example demonstrates the effect of the mole ratio of inorganic salt to nitrobenzene. Reaction conditions were comparable to those for Example 12, except that the mole ratio of KCI to nitrobenzene was varied. The results in Tabie 19 indicate the addition of only a small amount of inorganic salt will increase selectivity. Therefore, in situations where corrosion due to high salt level is a concern, at least a modest selectivity improvement can be obtained.
Table Mole ConversionSelectivity Yield, Ratio SaItINB % % p-NDPA 4-NDPA An RecrOther TMAH Only, 0 100.0 83.8 62.4 21.4 4.4 11.8 No Salt Added 4.66 g KCI 0.25 100.0 87.1 63.4 23.7 7.8 5.1 13.05 g 0.70 100.0 93.8 72.3 21.5 5.0 1.2 KCI
21.44 g 1.15 100.0 97.2 72.3 24.8 1.5 1.4 KCi This example demonstrates the effect of adding a non-salt compound on selectivity and conversion of nitrobenzene. Reaction conditions were comparable to those for Example 12. Betaine, i.e. (acetyl)trimethylammomnium hydroxide inner salt, is a salt formed by the acetate group with the positively charged tetraalkylammonium group. So despite the name, the compound does not actually have hydroxide associated with the tetraalkylammonium group.
However, when a strong base is added, betaine is converted to a compound that contains both an acetate salt group and a tetraalkylammonium hydroxide group.
So with TMAH, betaine is converted to a compound with a tetramethylammonium-acetate group and an (acetyl)trimethylammomnium hydroxide group. With KOH, the compound has a potassium -acetate group with the (acetyl)trimethyfammomnium hydroxide group. In the KOH case, the compound represents a metal organic salt and a organic base in one molecule.
Betaine is known in the literature to be a phase transfer compound or PTC
(Starks and Liotta, ibid), as it carries the inorganic or organic base into the organic phase.
The results in Table 20 show that betaine has only a modest effect on selectivity or conversion with TMAH. The results with betainelNB =1.15 are only equivalent to KCI/NB = 0.25. Furthermore, addition of an anion without an inorganic cation (am,monium acetate) is essentially ineffective. Therefore, the use of an inorganic salt or metal organic salt is the key to best results.
Table ConversionSelectivity Yieid, Mole Ratio% I p- 4- An Other to NB NDPA NDPA Recr TMAH Only, No 0 100.0 83.8 62.4 21.4 4.4 11.8 Salt or PTC Added 4.66 g KCI 0.25 100.0 87.1 63.4 23.7 7.8 5.1 21.44 g KCI 1.15 100.0 97.2 72.3 24.8 1.5 1.4 22.16 g Ammonium1.15 0.5 100.0 0.3 0.2 0.0 0.0 Acetate 33.68 g Betaine1.15 100.0 87.6 70.7 16.9 4.8 7.6 This example illustrates that use of partial oxidative conditions can give a significant increase of selectivity. Reaction conditions were comparable to those for Example 12, except as indicated. The results are shown in Table 21.
Reaction 1 had comparable conditions to those for Example 12 throughout. For Reaction 2, the air bleed was used only during nitrobenzene feed and was stopped when 75% of the feed was completed. For Reaction 3, the nitrobenzene feed time was shortened to 45 minutes and the hold time was increased to 60 minutes, while the air bleed was used only during the nitrobenzene feed time.
It is expected that higher selectivity will also be attained for sulfate, carbonate and nitrate by use of partial oxidative conditions.
Table 21 ConversionSelectivity Yield, p-NDPA 4-NDPA An Recr Other 16.70 g KF-199.9 84.8 67.3 17.4 4.2 11.0 16.70 g KF-2100.0 91.1 80.1 11.0 6.3 2.6 16.70 g KF-3100.0 93.8 83.2 10.6 4.3 1.9 This example shows that use of an oxidant with a strong base, which also functions as a phase transfer catalyst, can increase selectivity. The reactions were done with azeotropic removal of water and aniline.
Charged to a 500-mL round bottom flask equipped with a Teflon paddle stirrer, thermocouple, nitrobenzene feed tube and air bleed valve were: 145.28 grams aniline (1.56 moles) and 87.36 grams aqueous tetramethylammonium hydroxide solution (36.0%, 0.345 moles) for Runs 1 - 3. The mixture was heated for 30 minutes at 120 mm Hg and then nitrobenzene feed (36.93 grams, 0.30 moles) was started. The system pressure was held constant at 70 mm Hg throughout the reaction period. Temperature rose from about 66°C to about 80°C during the reaction period. Nitrobenzene was charged over about 80 minutes, after which the batch was held for 40 minutes at 70 mm Hg to insure completeness of reaction and then quenched with 25 mL water. Hydrogen peroxide was charged as 20.40 grams (0.03 moles) of a 5 wt.% aqueous solution concurrently with nitrobenzene. Since water can also affect selectivity, by protecting TMAH from degradation and shifting reaction equilibria, a control was run with 20.40 grams of water that was also fed concurrently with nitrobenzene.
Runs 4 - 7 had slightly different conditions. The main difference was starting with 25 wt.% TMAH with removal of water and some aniline in the reactor prior to the nitrobenzene feed. Air was added either during the entire nitrobenzene feed or for half of the feed time.
The results in Table 22 show that hydrogen peroxide gives a larger selectivity improvement than water alone, showing that use of an oxidant can be beneficial. The results also show that addition of air as oxidant over the entire reactor cycle has a deleterious effect on selectivity. However, a selectivity improvement is obtained when the air addition is limited to part of the reaction cycle, showing that partial oxidative conditions can be beneficial. These reactions were run somewhat wetter than the case for 100%
air in Table 18, which explains the lower selectivity in Table 18. Runs 4 and 5 show the excellent repeatability of the reactions, so that selectivity increases of 1 - 2% are significant.
Table 22 Conversion Selectivity Yield, TMAH as base/PTC % % p-NDPA 4-NDPA An Recr Other 1. No oxidant 100.0 93.3 86.3 7.0 4.6 2.1 2. Water only 100.0 94.9 89.3 5.5 3.4 1,8 3. Hydrogen Peroxide 100.0 96.1 89.7 6.4 1.9 2.0 4. No oxidant 100.0 92.3 86.5 5.8 5.9 1.8 5. No oxidant 100.0 92.2 86.2 6.0 6.1 1.7 6. Air, 100% NB Feed 99.7 89.4 79.0 10.1 7.4 3.2 7. Air, 50% NB Feed 100.0 94.5 88.4 6.2 4.2 1.3
Claims (67)
1. A method of producing 4-aminodiphenylamine or substituted derivatives thereof comprising the steps of:
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact;
(b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zone at a suitable time, pressure and temperature, in the presence of a mixture comprising a strong base, an oxidant and a phase transfer catalyst selected from the group of compounds defined by:
where R1, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from C1 to C20, (R4)e is hydrogen for e = 0, R4 is R1R2R3N+ for e = 1 or 2, Y is alkyl, aryl, alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, X is an anionic moiety of the form fluoride, chloride, hydroxide, sulfate, hydrogensulfate, acetate, formats, nitrate, phosphate, hydrogen phosphate, dihydrogen phosphate, oxalate, carbonate, borate, tartrate, citrate, malonate and mixtures of said compounds, where a = the valence of the anionic moiety (1, 2 or 3), b and c are whole number integers of value 1, 2 or 3 and d is a whole number integer of value 0 to 4; and (c) reducing the 4-aminodiphenylamine intermediate product of step (b) to produce 4-aminodiphenylamine or substituted derivatives thereof.
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact;
(b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zone at a suitable time, pressure and temperature, in the presence of a mixture comprising a strong base, an oxidant and a phase transfer catalyst selected from the group of compounds defined by:
where R1, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from C1 to C20, (R4)e is hydrogen for e = 0, R4 is R1R2R3N+ for e = 1 or 2, Y is alkyl, aryl, alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, X is an anionic moiety of the form fluoride, chloride, hydroxide, sulfate, hydrogensulfate, acetate, formats, nitrate, phosphate, hydrogen phosphate, dihydrogen phosphate, oxalate, carbonate, borate, tartrate, citrate, malonate and mixtures of said compounds, where a = the valence of the anionic moiety (1, 2 or 3), b and c are whole number integers of value 1, 2 or 3 and d is a whole number integer of value 0 to 4; and (c) reducing the 4-aminodiphenylamine intermediate product of step (b) to produce 4-aminodiphenylamine or substituted derivatives thereof.
2. The method of claim 1 wherein said phase transfer catalyst is selected from the group consisting of tetramethylammonium chloride, tetramethylammonium fluoride, tetramethylammonium hydroxide, bis-tetramethylammonium carbonate, tetramethylammonium formats and tetramethylammonium acetate; tetrabutylammonium hydrogensulfate and tetrabutylammonium sulfate; methyltributylammonium chloride; and benzyltrimethylammonium hydroxide, tricaprylmethylammonium chloride, tetrabutylammonium chloride, tetramethylammonium nitrate, cetyltrimethylammonium chloride and choline hydroxide.
3. The method of claim 1 wherein the molar ratio of phase transfer catalyst to nitrobenzene is from about 0.05:1 to about 1.2:1.
4. The method of claim 1 wherein said aniline derivative is selected from the group consisting of formanilide, phenylurea, carbanilide and thiocarbanilide.
5. The method of claim 1 wherein said aniline is a substituted aniline selected from the group consisting of 2-methoxyaniline, 4-methoxyaniline, 4-chloroaniline, p-toluidine, 4-nitroaniline, 3-bromoaniline, 3-bromo-4-aminotoluene, p-aminobenzoic acid, 2,4-diaminotoluene, 2,5-dichloroaniline, 1,4-phenylene diamine, 4,4'-methylene dianiline, 1,3,5-triaminobenzene, and mixtures thereof.
6. The method of claim 1 wherein substituted nitrobenzenes that may be used in accordance with the process of the present invention include o- and m-methylnitrobenzene, o- and m-ethylnitrobenzene, o- and m-methoxynitrobenzene, and mixtures thereof.
7. The method of claim 1 wherein said strong base is selected from the group consisting of potassium hydroxide, sodium hydroxide, cesium hydroxide,4 rubidium hydroxide and potassium-t-butoxide.
8. The method of claim 1 wherein the mole ratio of strong base to nitrobenzene is greater than about 1:1.
9. The method of claim 1 wherein the mole ratio of strong base to nitrobenzene is about 2:1 to about 6:1.
10. The method of claim 1 wherein said oxidant is free oxygen.
11. The method of claim 1 wherein said oxidant is an oxidizing agent.
12. The method of claim 11 wherein said oxidizing agent is a peroxide.
13. The method of claim 11 wherein said oxidizing agent is hydrogen peroxide.
14. The method of claim 11 wherein said oxidizing agent is nitrobenzene.
15. The method of claim 1 wherein said oxidant is present only for part of the time during which the aniline and nitrobenzene react.
16. The method of claim 1 wherein said reactive contact is carried out at a temperature of from about 20°C to about 150°C, a pressure in the range of from about 20 mbar to about 20 barg and a reaction time less than about 3.5 hours.
17. The method of claim 1 wherein the reaction of step (b) is carried out in the presence of not greater than about 10:1 moles water to moles nitrobenzene excluding water of hydration.
18. The method of claim 1 wherein said mixture comprising a strong base and a phase transfer catalyst is in aqueous solution and the reaction is carried out with a continuous distillation of aniline-water azeotrope.
19. The method of claim 18 wherein said phase transfer catalyst is tetramethylammonium bromide and said strong base comprises one or more inorganic bases.
20. The method of claim 1 wherein said reactive contact occurs in a suitable solvent system.
21. The method of claim 20 wherein said suitable solvent system comprises a polar aprotic solvent.
22. The method of claim 21 wherein said polar aprotic solvent is selected form the group consisting of dimethyl sulfoxide, benzyl ether, 1-Methyl-2-pyrrolidinone and N,N-dimethylformamide.
23. The method of claim 1 wherein the 4-aminodiphenylamine produced is reductively alkylated to an alkylated derivative of the 4-aminodiphenylamine.
24. A method of producing 4-aminodiphenylamine or substituted derivatives thereof comprising the steps of:
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact;
(b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zone at a suitable time, pressure and temperature in the presence of a mixture comprising an oxidant and a strong base that also functions as a phase transfer catalyst selected from the group of compounds defined by:
where R1, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from C1 to C20, (R4)e is hydrogen for e = 0, R4 is R1R2R3N+ for e = 1 or 2, Y is alkyl, aryl, alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, b and c are whole number integers of value 1, 2 or 3 and d is a whole number integer of value 0 to 4; and (c) reducing the 4-aminodiphenylamine intermediate product of step (b) to produce 4-aminodiphenylamine or substituted derivatives thereof.
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact;
(b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zone at a suitable time, pressure and temperature in the presence of a mixture comprising an oxidant and a strong base that also functions as a phase transfer catalyst selected from the group of compounds defined by:
where R1, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from C1 to C20, (R4)e is hydrogen for e = 0, R4 is R1R2R3N+ for e = 1 or 2, Y is alkyl, aryl, alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, b and c are whole number integers of value 1, 2 or 3 and d is a whole number integer of value 0 to 4; and (c) reducing the 4-aminodiphenylamine intermediate product of step (b) to produce 4-aminodiphenylamine or substituted derivatives thereof.
25. The method of claim 24 wherein said aniline derivative is selected from the group consisting of formanilide, phenylurea, carbanilide and thiocarbanilide.
26.The method of claim 24 wherein said aniline is a substituted aniline selected from the group consisting of 2-methoxyaniline, 4-methoxyaniline, 4-chloroaniline, p-toluidine, 4-nitroaniline, 3-bromoaniline, 3-bromo-4-aminotoluene, p-aminobenzoic acid, 2,4-diaminotoluene, 2,5-dichloroaniline, 1,4-phenylene diamine, 4,4'-methylene dianiline, 1,3,5-triaminobenzene, and mixtures thereof.
27. The method of claim 24 wherein substituted nitrobenzenes that may be used in accordance with the process of the present invention include o- and m-methylnitrobenzene, o- and m-ethylnitrobenzene, o- and m-methoxynitrobenzene, and mixtures thereof.
28. The method of claim 24 wherein said strong base that also functions as a phase transfer catalyst comprises tetramethylammonium hydroxide and/or benzyltrimethylammonium hydroxide.
29. The method of claim 24 wherein the mole ratio of strong base to nitrobenzene is greater than about 1:1.
30. The method of claim 24 wherein the mole ratio of strong base to nitrobenzene is about 2:1 to about 6:1.
31. The method of claim 24 wherein said oxidant is an oxidizing agent.
32. The method of claim 31 wherein said oxidizing agent is a peroxide.
33. The method of claim 31 wherein said oxidizing agent is hydrogen peroxide.
34. The method of claim 24 wherein said oxidant is present only for part of the time during which the aniline and nitrobenzene react.
35. The method of claim 34 wherein said oxidant is free oxygen.
36. The method of claim 24 wherein said reactive contact is carried out at a temperature of from about 20°C to about 150°C, a pressure in the range of from about 20 mbar to about 20 barg and a reaction time less than about 3.5 hours.
37. The method of claim 24 wherein the reaction of step (b) is carried out in the presence of not greater than about 10:1 moles water to moles nitrobenzene excluding water of hydration.
38. The method of claim 24 wherein said reactive contact occurs in a suitable solvent system.
39. The method of claim 38 wherein said suitable solvent system comprises a polar aprotic solvent.
40. The method of claim 39 wherein said polar aprotic solvent is selected form the group consisting of dimethyl sulfoxide, benzyl ether, 1-Methyl-2-pyrrolidinone and N,N-dimethylformamide.
41. The method of claim 24 wherein the 4-aminodiphenylamine produced is reductively alkylated to an alkylated derivative of the 4-aminodiphenylamine.
42. A method of producing 4-aminodiphenylamine or substituted derivatives thereof comprising the steps of:
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact; and (b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zone at a suitable time, pressure and temperature, in the presence of a mixture comprising an inorganic salt or metal organic salt, or mixtures thereof, having a cation that would be a suitable cation of a strong inorganic base, an oxidant and one or more of an organic base selected from the group of compounds defined by:
where R1, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from 1 to about 20 carbon atoms, a is a whole number integer of value 0, 1, 2 or 3, (R4)e is hydrogen for e = 0, is R1R2R3N+ for e = 1, 2, or 3, X is an anion capable of abstracting a proton from the nitrogen of an aniline or aniline derivative, Y is alkyl, aryl, alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, where a = the valence of the anionic moiety and is a whole number integer of 1, 2, 3 or 4, b and c are whole number integers of value 1, 2, 3 or 4 and d is a whole number integer of value 0, 1, 2, 3 or 4, said mixture not including a reaction product of betaine and a strong inorganic base; and (c) reducing the 4-aminodiphenylamine intermediate product of step (b) to produce 4-aminodiphenylamine or substituted derivatives thereof.
(a) bringing an aniline or aniline derivative and nitrobenzene or nitrobenzene derivative into reactive contact; and (b) obtaining a 4-aminodiphenylamine intermediate product by reacting the aniline or aniline derivative and nitrobenzene or nitrobenzene derivative in a confined zone at a suitable time, pressure and temperature, in the presence of a mixture comprising an inorganic salt or metal organic salt, or mixtures thereof, having a cation that would be a suitable cation of a strong inorganic base, an oxidant and one or more of an organic base selected from the group of compounds defined by:
where R1, R2, R3 are the same or different and selected from any straight chain or branched alkyl group containing from 1 to about 20 carbon atoms, a is a whole number integer of value 0, 1, 2 or 3, (R4)e is hydrogen for e = 0, is R1R2R3N+ for e = 1, 2, or 3, X is an anion capable of abstracting a proton from the nitrogen of an aniline or aniline derivative, Y is alkyl, aryl, alkyl aryl or benzyl and substituted derivatives thereof, Z is a substituent selected from the group consisting of hydroxyl, halo, and other hetero atoms, where a = the valence of the anionic moiety and is a whole number integer of 1, 2, 3 or 4, b and c are whole number integers of value 1, 2, 3 or 4 and d is a whole number integer of value 0, 1, 2, 3 or 4, said mixture not including a reaction product of betaine and a strong inorganic base; and (c) reducing the 4-aminodiphenylamine intermediate product of step (b) to produce 4-aminodiphenylamine or substituted derivatives thereof.
43.The method of claim 42 wherein said organic base is a quaternary ammonium hydroxide selected from the group consisting of tetramethylammonium hydroxide, tetrabutylammonium hydroxide, methyltributylammonium hydroxide, benzyltrimethylammonium hydroxide, tricaprylmethylammonium hydroxide, cetyltrimethylammonium hydroxide and choline hydroxide and equivalent quaternary ammonium alkoxides, acetates, carbonates, bicarbonates, cyanides, phenolics, phosphates, hydrogen phosphates, hypochlorites, borates, hydrogen borates, dihydrogen borates, sulfides, silicates, hydrogen silicates, dihydrogen silicates and trihydrogen silicates.
44. The method of claim 42 wherein the molar ratio of organic base used with an inorganic salt or metal organic salt to nitrobenzene is greater than or equal to about 1:1.
45.The method of claim 42 wherein the molar ratio of organic base to nitrobenzene is from about 1.1:1 to about 6:1.
46. The method of claim 42 wherein the mole ratio of inorganic salt or metal organic salt to nitrobenzene is from about 0.05:1 to about 6.5:1.
47. The method of claim 42 wherein the mole ratio of inorganic salt or metal organic salt to organic base is greater than or equal to about 1:1.
48. The method of claim 42 wherein said aniline derivative is selected from the group consisting of formanilide, phenylurea, carbanilide and thiocarbanilide.
49. The method of claim 42 wherein said aniline is a substituted aniline selected from the group consisting of 2-methoxyaniline, 4-methoxyaniline, 4-chloroaniline, p-toluidine, 4-nitroaniline, 3-bromoaniline, 3-bromo-4-aminotoluene, p-aminobenzoic acid, 2,4-diaminotoluene, 2,5-dichloroaniline, 1,4-phenylene diamine, 4,4'-methylene dianiline, 1,3,5-triaminobenzene, and mixtures thereof.
50. The method of claim 42 wherein substituted nitrobenzenes that may be used in accordance with the process of the present invention include o- and m methylnitrobenzene, o- and m-ethylnitrobenzene, o- and m-methoxynitrobenzene, and mixtures thereof.
51. The method of claim 42 wherein said inorganic salt or metal organic salt used in conjunction with an organic base is selected from the group consisting of the fluoride, chloride, bromide, sulfate, hydrogen sulfate, nitrate, phosphate, formate, acetate and carbonate salts of cesium, rubidium, potassium and sodium and mixtures thereof.
52. The method of claim 42 wherein said oxidant is free oxygen.
53. The method of claim 42 wherein said oxidant is an oxidizing agent.
54. The method of claim 53 wherein said oxidizing agent is a peroxide.
55. The method of claim 53 wherein said oxidizing agent is hydrogen peroxide.
56. The method of claim 53 wherein said oxidizing agent is nitrobenzene.
57. The method of claim 42 wherein said oxidant is present only for part of the time during which the aniline and nitrobenzene react.
58. The method of claim 42 wherein said reactive contact is carried out at a temperature of from about 20°C to about 150°C, a pressure in the range of from about 20 mbar to about 20 barg and a reaction time less than about 3.5 hours.
59. The method of claim 42 wherein the reaction of step (b) is carried out in the presence of not greater than about 10:1 moles water to moles nitrobenzene excluding water of hydration.
60. The method of claim 42 wherein said mixture comprising an organic base and an inorganic salt or metal organic salt is in aqueous solution and the reaction is carried out with a continuous distillation of aniline-water azeotrope.
61. The method of claim 42 wherein said reactive contact occurs in a suitable solvent system.
62. The method of claim 61 wherein said suitable solvent system comprises a polar aprotic solvent.
63. The method of claim 62 wherein said polar aprotic solvent is selected form the group consisting of dimethyl sulfoxide, benzyl ether, 1-Methyl-2-pyrrolidinone and N,N-dimethylformamide.
64. The method of claim 42 wherein the 4-aminodiphenylamine produced is reductively alkylated to an alkylated derivative of the 4-aminodiphenylamine.
65. The method of claim 42 wherein X of formula III is selected from the group of anions consisting of hydroxide, alkoxide, acetate, carbonate, bicarbonate, cyanide, phenolic, phosphate, hydrogen phosphate, hypochlorite, borate, hydrogen borate, dihydrogen borate, sulfide, silicate, hydrogen silicate, dihydrogen silicate and trihydrogen silicate.
66. The method of claim 42 wherein said organic base is tetramethylammonium hydroxide, said inorganic salt includes a halide anion and the reaction is carried in aqueous solution with a continuous distillation of aniline-water azeotrope.
67. The method of claim 66 wherein said halide anion is chloride.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA2690106A CA2690106A1 (en) | 2001-07-23 | 2002-07-09 | Process for preparing 4-aminodiphenylamines |
| CA002675685A CA2675685A1 (en) | 2001-07-23 | 2002-07-09 | Process for preparing 4-aminodiphenylamines |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/911,058 US6395933B1 (en) | 2001-07-23 | 2001-07-23 | Process for preparing 4-aminodiphenylamine intermediates |
| US09/911,058 | 2001-07-23 | ||
| US10/143,478 | 2002-05-10 | ||
| US10/143,478 US6583320B2 (en) | 2001-07-23 | 2002-05-10 | Process for preparing 4-aminodiphenylamine intermediates |
| PCT/US2002/021508 WO2003010126A1 (en) | 2001-07-23 | 2002-07-09 | Process for preparing 4-aminodiphenylamine |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002675685A Division CA2675685A1 (en) | 2001-07-23 | 2002-07-09 | Process for preparing 4-aminodiphenylamines |
| CA2690106A Division CA2690106A1 (en) | 2001-07-23 | 2002-07-09 | Process for preparing 4-aminodiphenylamines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2454603A1 true CA2454603A1 (en) | 2003-02-06 |
Family
ID=26841060
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002454603A Abandoned CA2454603A1 (en) | 2001-07-23 | 2002-07-09 | Process for preparing 4-aminodiphenylamine |
Country Status (15)
| Country | Link |
|---|---|
| EP (1) | EP1414782A1 (en) |
| JP (1) | JP4603260B2 (en) |
| CN (1) | CN100546972C (en) |
| AU (1) | AU2002315530B2 (en) |
| BR (1) | BR0211391B1 (en) |
| CA (1) | CA2454603A1 (en) |
| HU (1) | HUP0501066A2 (en) |
| IL (1) | IL159994A0 (en) |
| MX (1) | MXPA04000665A (en) |
| NO (1) | NO20040292L (en) |
| PL (1) | PL206080B1 (en) |
| RS (1) | RS3904A (en) |
| RU (1) | RU2280640C2 (en) |
| TW (1) | TWI265919B (en) |
| WO (1) | WO2003010126A1 (en) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6395933B1 (en) * | 2001-07-23 | 2002-05-28 | Flexsys America, L.P. | Process for preparing 4-aminodiphenylamine intermediates |
| US7183439B2 (en) * | 2002-12-10 | 2007-02-27 | Flexsys America L.P. | Process for preparing 4-aminodiphenylamine intermediates |
| US7176333B2 (en) | 2003-07-04 | 2007-02-13 | Sinorgchem Company, Shandong | Process for preparing 4-aminodiphenylamine |
| US8486223B2 (en) | 2003-07-04 | 2013-07-16 | Jiangsu Sinorgchem Technology Co., Ltd. | Falling film evaporator |
| JP4500302B2 (en) | 2003-07-04 | 2010-07-14 | チアンス・シノケム・テクノロジー・カンパニー・リミテッド | Method for producing 4-aminodiphenylamine |
| US8686188B2 (en) | 2003-07-04 | 2014-04-01 | Jiangsu Sinorgchem Technology Co., Ltd. | Process for preparing 4-aminodiphenylamine |
| KR100621310B1 (en) * | 2005-05-16 | 2006-09-06 | 금호석유화학 주식회사 | Method for preparing 4-aminodiphenylamine |
| JP4876707B2 (en) * | 2006-05-10 | 2012-02-15 | 住友化学株式会社 | Method for producing 4-nitrosodiphenylamine and 4-nitrodiphenylamine |
| KR100932208B1 (en) * | 2009-05-21 | 2009-12-16 | 엘아이지넥스원 주식회사 | Sdr apparatus based on sca and method for executing waveform in the apparatus |
| CN101717339A (en) * | 2009-12-08 | 2010-06-02 | 江苏扬农化工集团有限公司 | Double quaternary ammonium base compound and preparation method as well as application thereof |
| CN101830811B (en) * | 2010-02-23 | 2013-04-03 | 江苏扬农化工集团有限公司 | Preparation method of 4-aminodiphenylamine |
| WO2011148976A1 (en) * | 2010-05-26 | 2011-12-01 | 住友化学株式会社 | Method for producing 4-nitrodiphenylamine |
| CN102372640A (en) * | 2010-08-20 | 2012-03-14 | 中国石油化工集团公司 | Method for preparing 4-nitrodiphenylamine and 4-nitrosodiphenylamine |
| CN102344376B (en) * | 2011-08-17 | 2014-04-02 | 中国石油化工股份有限公司 | Method for preparing p-aminodiphenylamine |
| RU2553984C2 (en) * | 2013-02-28 | 2015-06-20 | Олег Александрович ГОДЗОЕВ | Method of obtaining 4-aminodiphenylamine and its alkylated derivatives |
| CN103819346B (en) * | 2014-03-17 | 2015-11-04 | 山东尚舜化工有限公司 | A kind of production unit of precursor of 4-ADPA and production technique |
| CN108558675A (en) * | 2018-04-25 | 2018-09-21 | 南通理工学院 | Synthesis method of 4-aminodiphenylamine |
| CN111689866A (en) * | 2019-03-15 | 2020-09-22 | 中石化南京化工研究院有限公司 | Preparation method of tower reaction RT base |
| RU2706682C1 (en) * | 2019-07-24 | 2019-11-20 | Вахтанг Нодарович Лемонджава | Apparatus for monitoring and regulating the process of defrosting plasma and blood cells |
| CN113527111B (en) * | 2020-04-10 | 2023-09-15 | 中国石油化工股份有限公司 | Method for preparing RT (reverse transcription) sauce by normal pressure condensation |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4463191A (en) * | 1983-09-26 | 1984-07-31 | The Goodyear Tire & Rubber Company | Process for the reductive alkylation of aromatic nitro-containing compounds with ketones or aldehydes |
| DE3620639A1 (en) * | 1986-06-20 | 1987-12-23 | Bayer Ag | Process for the preparation of 4-nitrodiphenylamines |
| US5117063A (en) * | 1991-06-21 | 1992-05-26 | Monsanto Company | Method of preparing 4-aminodiphenylamine |
| EP0566783A1 (en) * | 1992-04-21 | 1993-10-27 | Akzo N.V. | Process for the production of nitrodiarylamines |
| JPH07149695A (en) * | 1993-09-30 | 1995-06-13 | Seiko Kagaku Kk | Production of 4-aminodiphenylamine |
| DE4427249A1 (en) * | 1994-08-02 | 1996-02-08 | Bayer Ag | Process for the preparation of nitro-substituted arylamines |
| DE19600722A1 (en) * | 1996-01-11 | 1997-07-17 | Bayer Ag | Process for the preparation of optionally substituted 4-aminodiphenylamines |
| US5977411A (en) * | 1997-06-10 | 1999-11-02 | Flexsys America L.P. | Catalytic hydrogeneration of nitrobenzene to 4-aminodiphenylamine in the presence of a hydroxyl compound and a solvent |
| SK283209B6 (en) * | 1998-12-11 | 2003-03-04 | Duslo, A. S. | Preparation method for 4-aminodiphenylamine |
| KR100298572B1 (en) * | 1999-08-19 | 2001-09-22 | 박찬구 | The method for preparing 4-nitrodiphenylamine and 4-nitrosodiphenylamine from carbanilide |
-
2002
- 2002-07-09 CA CA002454603A patent/CA2454603A1/en not_active Abandoned
- 2002-07-09 EP EP02742396A patent/EP1414782A1/en not_active Withdrawn
- 2002-07-09 AU AU2002315530A patent/AU2002315530B2/en not_active Ceased
- 2002-07-09 JP JP2003515487A patent/JP4603260B2/en not_active Expired - Lifetime
- 2002-07-09 CN CNB028164474A patent/CN100546972C/en not_active Expired - Lifetime
- 2002-07-09 RS YU3904A patent/RS3904A/en unknown
- 2002-07-09 HU HU0501066A patent/HUP0501066A2/en unknown
- 2002-07-09 RU RU2004105163/04A patent/RU2280640C2/en not_active IP Right Cessation
- 2002-07-09 MX MXPA04000665A patent/MXPA04000665A/en active IP Right Grant
- 2002-07-09 BR BRPI0211391-0A patent/BR0211391B1/en active IP Right Grant
- 2002-07-09 PL PL374267A patent/PL206080B1/en unknown
- 2002-07-09 WO PCT/US2002/021508 patent/WO2003010126A1/en active Application Filing
- 2002-07-09 IL IL15999402A patent/IL159994A0/en unknown
- 2002-07-22 TW TW091116246A patent/TWI265919B/en not_active IP Right Cessation
-
2004
- 2004-01-22 NO NO20040292A patent/NO20040292L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| RU2280640C2 (en) | 2006-07-27 |
| RU2004105163A (en) | 2005-08-10 |
| CN100546972C (en) | 2009-10-07 |
| TWI265919B (en) | 2006-11-11 |
| BR0211391B1 (en) | 2013-05-14 |
| PL374267A1 (en) | 2005-10-03 |
| MXPA04000665A (en) | 2004-04-05 |
| PL206080B1 (en) | 2010-06-30 |
| CN1545497A (en) | 2004-11-10 |
| NO20040292L (en) | 2004-03-19 |
| WO2003010126A1 (en) | 2003-02-06 |
| EP1414782A1 (en) | 2004-05-06 |
| BR0211391A (en) | 2006-05-23 |
| IL159994A0 (en) | 2004-06-20 |
| AU2002315530B2 (en) | 2008-05-22 |
| JP2005515163A (en) | 2005-05-26 |
| JP4603260B2 (en) | 2010-12-22 |
| HUP0501066A2 (en) | 2006-09-28 |
| RS3904A (en) | 2006-12-15 |
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| EEER | Examination request | ||
| FZDE | Discontinued |