US3488397A

US3488397A - Nitration of alkyl benzenes with nitric and phosphoric acids

Info

Publication number: US3488397A
Application number: US676607A
Authority: US
Inventors: Christer Lennart Hakansson; Arne Arvid Arvidsson; Ingar Loken
Original assignee: Bofors AB
Current assignee: Saab Bofors AB
Priority date: 1966-10-20
Filing date: 1967-10-19
Publication date: 1970-01-06
Anticipated expiration: 1987-01-06
Also published as: GB1207384A; DE1643600B2; CH485643A; DE1643600C3; DE1643600A1; SE305862B

Description

United States Patent 3,488,397 NITRATION OF ALKYL BENZENES WITH NITRIC AND PHOSPHORIC ACIDS Christer Lennart Hakanssou, Bofors, and Arne Arvid Arvidsson and Ingar Loken, Karlskoga, Sweden, assignors to Aktiebolaget Bofors, Bofors, Sweden No Drawing. Filed Oct. 19, 1967, Ser. No. 676,607 Claims priority, application Sweden, Oct. 20, 1966,

Int. Cl. C07c 79/10 US. Cl. 260-645 12 Claims ABSTRACT OF THE DISCLOSURE This disclosure teaches a process for nitrating alkylsubstituted aromatic compounds (particularly toluene) in such a manner that a greater yield of p-isomers is obtained, as compared with o and m-isomers, than had heretofore been achieved. Nitration is here carried out with nitric acid in the presence of phosphoric acid. The concentration and quantity of the phosphoric acid are chosen in such a way that after the reaction the P 0 content thereof is not more than 82% and preferably between 62% and 76%. Sulphuric acid may also be present, preferably with its quantity not more than 80% that of phosphoric acid. v

BACKGROUND OF THE INVENTION Usually nitrations of aromatic compounds have been carried out with the use of a mixture of nitric acid and sulphuric acid, and in the mononitro compounds formed, the portion of o-isomers has generally been largest. Thus, for instance, when nitrating toluene, the ratio by percentage among 0, m and p-nitrotoluene has been approximately 58.5/4.5/37.0. This isomer relationship has been almost independent of the reaction conditions.

During recent years, however, there has been an increased demand for p-nitrotoluene, for instance as a raw material for optical brighteners. There has also been an increased demand for the p-isomer for other mononitro alkyl benzenes. Thus, p-nitroethyl-benzene for example has become an important raw material for chloro-amphenicol, an antibiotic. Accordingly, it has become of inte-rest to endeavor to carry out nitration of aromatic compounds in such a way that an increased yield of p-isomer is obtained. Among other things, it has beenpro'posed to use a sulphonated ion exchanger or aromatic sulphonic acids instead of sulphuric acid. These methods have also led to a greater yield of pisomer, but they have proven to be uncertain when used on an industrial scale, among other things owing to the difficulty in recovering and recirculating the comparatively expensive auxiliary chemicals. Another proposal for achieving a higher yield of p-isomer involves nitration with alkyl nitrates in the presence of polyphosphoric acid. This method cannot have any commercial significance either, because it is altogether too expensive. Attempts have also been made to nitrate toluene with nitric acid in the presence of polyphosphoric acid, whereby a certain although somewhat smaller increase of p-nitrotoluene yield has been obtained. In these attempts it has proven to be most appropriate to use polyphosphoric acid with a concentration corresponding to 83% phosphorus pentoxide (P 0 The explanation of the effect of the polyphosphoric acid on the isomer ratio must in all probability be that the primary attack at the nitration was obtained through a nitronium ion,

which exists in association with a molecule of a polymer phosphoric acid. The great space which such an association product requires has been assumed to involve a steric hindrance for the nitration in o-position to the alkyl group. The use of polyphosphoric acid in accordance with 3,488,397 Patented Jan. 6, 1970 SUMMARY OF INVENTION Through the present invention, it has become possible to carry out nitration of alkyl-substituted aromatic compounds in a way that can be performed technically, so that a greater yield of p-isomer is obtained than when earlier methods are used. Through the method, according to the present invention, it is possible in a simple and economically satisfactory way to carry out nitrations of the desired kind, without any inconveniencing quantities of undesirable dinitro compounds arising, and without encountering any particular difliculties in the recovery of the spent acid. It has been discovered, quite unexpectedly, that the desired increase of the yield of p-nitro alkyl benzene can be obtained with phosphoric acid of a considerably lower concentration than has previously been known, and the desired effect can be obtained at P 0 contents corresponding to pure ortho-phosphoric acid, or, in fact, diluted ortho-phosphoric acid of ordinary commercial quality. At the same time, it has been discovered, quite unexpectedly, that the desired increase of the yield of p-isomer is retained if the nitration is carried out in a mixture of phosphoric acid and sulphuric acid.

DESCRIPTION OF THE PREFERRED EMBODIMENT When nitrating in the presence of phosphoric acid, as well as in the presence of sulphuric acid, it is the composition of the spent acid obtained that is decisive for the result of the nitration. In the following, the R 0 content of the phosphoric acid which is present in the spent acid (i.e. the part of the spent acid which does not consist of nitric acid) has been designated as the P 0 content in the spent acid, which corresponds to the mode of expression that is the practice in conventional nitration in the presence of sulphuric acid.

The method of nitrating alkyl-substituted aromatic compounds, particularly toluene, in such a way that a greater portion of p-isomer is obtained than when earlier methods are used, is characterized according to the present invention in that the nitration is carried out with nitric acid in the presence of phosphoric acid, the concentration and quantity of which is chosen in such a way that after the reaction the P 0 content of the phosphoric acid to not more than 82%. The phosphoric acid should particularly be chosen so that the P 0 content after the reaction does not exceed 76%, and it can appropriately amount to between 62 and 76%. It can also be appropriate that the acid mixture used for the nitration also contains sulphuric acid, and the quantity of sulphuric acid should then amount to not more than 80% of the quantity of phosphoric acid.

The invention will now be described in more detail, with reference to some experiments, accounted for as examples of carrying out the method.

Examples 1-7 In Example 1, to 5.65 g. of toluene there was added during the course of 15 minutes and with intensive stirring, 41.5 g. of nitration acid, consisting of 4 g. of 99% nitric acid and 37.5 g. of phosphoric acid containing 73% P 0 The stirring was thereafter continued for 40 minutes, and during the whole of the experiment the temperature was kept at 30i1 C. The reaction mixture was thereafter poured out on 400 g. of ice, after which extraction with 3 X 20 ml. of chloroform took place. The chloroform phase was thereafter washed with water and analyzed with gas chromatography.

The results of the experiment will be noted from the attached table, in which 6 other experiments have likewise been accounted for, which other experiments were carried out in an entirely similar way, but in which there were certain variations as regards the molar ratio between nitric acid and toluene and the concentration of phosphoric acid and the reaction temperature. Thus, in Example 1, a molar excess of approximately 2% of nitric acid in relation to the toluene was used, while for experiments 2-7, nitric acid with approximately 6% deficit was used.

As will be noted from the table, at Example 1, a considerably greater portion of p-isomer was obtained than at the conventional nitration with nitric acid and sulphur acid, in which the ratio p-nitrotoluene (PNT) to o-nitrotoluene (ONT) is approximately 0.63, while said ratio in Example 1 amounted to 1.11.

In Example 2, the P content of spent acid is 62.7, and even at this low concentration, there is a noticeable improvement as regards the increased yield of p-isomer.

In Example 3, the P 0 content in the spent acid has been increased to 69.0%, and thereby also a considerable improvement of the yield of p-isomer has been obtained in relation to Example 2.

Also in Example 4, the increase of the P 0 content in the spent acid (to 76.6) has increased the portion of p-isomer in the end product, but at the same time a certain, although comparatively small, quantity of dinitrotoluene (DNT) has been formed.

If, as in Example 5, the P 0 content in the spent acid is allowed to amount to 82.0%, the quantity of dinitrotoluene will increase quite considerably, and therefore the P 0 content must not be allowed to exceed 82%. In Example 5, the quantity of p-nitrotoluene in relation to the quantity of o-nitrotoluene has further increased, but this is associated with the fact that at the dinitration, which is not desired, it is particularly the o-nitrotoluene which is consumed.

Example 6 shows an experiment in which the reaction temperature has been reduced to 10 C., which does not seem to have had any noticeable effect on the relaiton between the quantities of pand o-isomers.

In Example 7, finally, the reaction temperature has been increased to 70 C., and a comparison with Example 3 shows that the decrease in the relation of p-isomer to o-isomer is comparatively insignificant.

From the table, it can be seen that the P 0 content in the spent acid should amount to not more than 82%, but should appropriately not be more than 76%, in order that the desired increase of the quantity of p-nitrotoluene may be obtained without altogether too great dinitration. It will also be noted from the table that the influence of the reaction temperature is insignificant when this is varied within reasonable limits. Nor does a slight excess or deficit of nitric acid seem to have any noticeable influence on the result.

Example 8 To 7.1 g. of ethylbenzene was added during the course of minutes, with intensive stirring, 53 g. of nitration acid consisting of 4 g. of nitric acid and 49 g. of phosphoric acid with 76.7% P 0 This involves that the molar ratio between the nitric acid and the ethylbenzene shows as deficit of nitric acid of approximately 5%. After the addition of the ingredients, the stirring was continued for 40 minutes, and during this time, as well as during the entire experiment, the temperature was kept at 30 C. In the same way as described in Example 1, the reaction mixture was thereafter poured out on ice and extracted with chloroform, after which the chloroform phase was washed with water and analyzed with gas chromatography. This analysis gave the following results:

Percent o-Nitro-ethylbenzene 40.6 m-Nitro-ethylbenzene 3.7 p-Nitro-ethylbenzene 55.7

The ratio of p/o-isomer thus became 1.37, which is considerably better than the result obtained at the nitration in the conventional way with nitric acid and sulphuric acid, at which said ratio will be approximately 1.08.

The P 0 content in the spent acid amounted to 75.0%.

Example 9 To 7.1 g. of isopropylbenzene was added during the course of 45 minutes and with intensive stirring 53 g. of nitration acid with the same composition as per example 8, after which the stirring was continued for 10 minutes at 3540 C. During the actual addition of the ingredients, the temperature was approximately 50 C. In this case, the gas chromatography gave a ratio between p/o-isomer of 3.03, which is considerably higher than the same value 2.08 for the corresponding conventional nitration with nitric acid and sulphuric acid.

For this experiment, a 10% excess of the nitric acid was used, and the P 0 content in the spent acid was 76.3%.

Example 10 To 0.2 g. of toluene was added during the course of 15 minutes with intensive stirring 53 g. of nitration acid consisting of 4 g. of nitric acid and 49 g. of phosphoric acid with 82% P 0 This addition of ingredients involves that to each mole of toluene is added approximately 29 moles of nitric acid. After the addition of the ingredients, the stirring was continued for 1 hour, and during the whole experiment the temperature was kept at 30 C. The P 0 content in the spent acid was 81.45%. Through gas chromatography, the following composition of the product was obtained:

Percent 2,6-dinitrotoluene (2,6-DNT) 9.6 2,4-dinitrotoluene (2,4-DNT) 86.4 Other dinitrotoluenes 4.0

Percent 2,6-DNT 20 Other dinitrotoluenes 4.0

Example 11 To 5 g. of o-nitrotoluene was added during the course of 15 minutes and with intensive stirring 53.6 g. of nitration acid consisting of 4.6 g. of nitric acid and 49 g. of phosphoric acid with 82.2% P 0 This addition of ingredients involves that to each mole of o-nitrotoluene is added 2 moles of nitric acid. After the addition of the ingredients, the stirring was continued for 1 hour, and during the whole of the experiment the temperature was kept at 30 C. This P 0 content in the spent acid was 81%. The analysis with gas chromatography gave the following results:

Percent 2,4-DNT 72.9 2,6-DNT 27.1

At conventional nitration with nitric acid and sulphuric acid, the following is obtained:

Percent 2,4-DNT 67 2,6-DNT 33 The portion of 2,4-DNT has thus, in the experiment here described, been improved in relationto the yield with conventional nitration.

Percent 3,4-DNT 64.0 2,3-DNT 24.3 2,5-DNT 11.7

With the corresponding nitration carried out which conventional nitration acid consisting of nitric acid and sulphuric acid, the following result was obtained:

Percent 3,4-DNT 49.9 2,3-DNT 38.0 2,5-DNT 12.0

If the compositions of the two products are compared, it will be clearly noted that the content of 3,4-DNT increased at the expense of the 2,3-DNT. The content of P in the spent acid was 81.0%.

Example 13 To 12 g. of toluene was added during the course of 15 minutes and with intensive stirring 57.9 g. of nitration acid consisting of 4 g. of nitric acid, 49 g. of phosphoric acid with 78.4% P 0 and 4.9 g. of sulphuric acid (96.5 This addition of ingredients involves that approximately 0.5 mole of nitric acid corresponded to each mole of toluene. After the addition of the ingredients, the stirring was continued for 40 minutes. During the whole of the experiment that temperature was kept at 30 C. Through gas chromatography the composition of the products was fixed at:

Percent ONT 40.4

MNT 4.3

PNT 51.6

DNT 3.7

Percent P 0 6 Example 14 To 6.15 g. of toluene was added during the course of 15 minutes and with intensive stirring, 92.2 g. of nitration acid consisting of 4 g. of nitric acid, 49' g. of phosphoric acid with 75.2% P 0 and 39.2 g. of sulphuric acid (96.5%). With this composition, there was thus an approximate 6% deficit of nitric acid in relation to the toluene. This stirring was continued for 40 minutes and the temperature was C., and the P 0 content in the spent acid was 71.4%. Gas chromatography showed the following product composition Percent ONT 41.0 MNT 3.0 1 PNT 45.1 DNT 10.9

' The ratio PNT to ONT was thus 1.10, or practically the same as for experiment 6, in which the P 0 content of the spent acid was approximately the same. However, a comparatively significant formation of dinitrotoluene had taken place, and the addition of sulphuric acid corresponding to 80% of the phosphoric acid should therefore appropriately not be carried much farther.

An addition of sulphuric acid as described in the two last-mentioned experiments can be advantageous, as it prevents crystallization of the phosphoric acid, which can otherwise involve technical problems, particularly with P 0 contents of between 78 and 82%.

From the experiments described above, it will be noted that even if the present method has its greatest significance for toluene, it can also be used to advantage for other alkyl-substituted aromatic compounds, for instance ethylbenzene and isopropylbenzene, and an increased yield of the p-isomer in relation to the result with conventional nitration with nitric acid and sulphuric acid is then obtained.

If the reaction is carried out so that dinitration takes place, an increased yield of 2,4-DNT will be obtained, and if the o-nitrotoluene and the m-nitrotoluene is nitrated according to the invention, the quantities of 2,4 and 3,4-DNT will increase. In all cases, the nitration in pposition will take place to a greater extent that at conventional nitration.

Nitration according to the invention can take place advantageously with a continuous procedure, and it has proven possible, for instance, for continuous mononitration of the toluene, to use apparatus which has originally been designed for conventional nitration with nitric acid and sulphuric acid.

Recovery of the phosphoric acid in the spent acid can, in principle, take place in the same way as for sulphuric acid, i.e. by heating and distilling 011 the water.

Grams added Reaction In phos- Phostemperaphoric Product composition, percent Turnover Ratio, phoric Nitric ture, acid In spent of toluene PNT/ acid acid Toluene 0. added acid MNT ONT PNT DNT percent ONT The ratio of PNT to ONT is 1.28 or somewhat higher than as per Example 4, in which the P 0 content of the spent acid was practically the same as for this experiment, in which it amounted to 76.4%. Thus, the addition of sulphuric acid corresponding to 10% of the phosphoric acid has not had any detrimental elfect on the distribution of isomers, although there has been a certain, slight increase of the quantity of DNT.

It will 'be apparent to those skilled in the nitrating of alkyl-substituted aromatic compounds that deviations may be made from the disclosed examples without departing from the main theme of invention set forth in the following claims.

What is claimed is:

1. A process for nitrating an alkyl-substituted aromatic compound in such a way that the p-isomer yield is optimized and comprising the step of carrying out the nitration with nitric acid in the presence of phosphoric acid, with the concentration and quantity of the phosphoric acid chosen in such a way that after the reaction the P content thereof is not more than 82%.

2. The process according to claim 1 with the P 0 content not more than 76%.

3. The process according to claim 2 with the P 0 content between 62% and 76%.

4. The process according to claim 1 with the alkylsubstituted aromatic compound toluene.

5. The process according to claim 2 with the alkylsubstituted aromatic compound toluene.

6. The process according to claim 3 with the alkylsubstituted aromatic compound toluene.

7. A process for nitrating an alkyl-substituted aromatic compound in such a way that the p-isomer yield is optirnized and comprising the step of carrying out the nitration with nitric acid in the presence of phosphoric acid and sulphuric acid, with the concentration and quantity of the phosphoric acid chosen in such a way that after the reaction the P 0 content thereof is not more than 82%.

8. The process according to claim 7 with the P 0 content not more than 76%.

9. The process according to claim 7 with the P 0 content between 62% and 76%.

10. The process according to claim 7 with the quantity of sulphuric acid not more than 80% that of phosphoric acid.

11. The process according to claim 8 with the quantity of sulphuric acid not more than 80% that of the phosphoric acid.

12. The process according to claim 9 with the quantity of sulphuric acid not more than 80% that of the phosphoric acid.

References Cited Urbanski; Chemistry and Technology of Explosives, The Macmillan Co., New York, 1964, pp. 271-275 and 340-344.

LELAND A. SEBASTIAN, Primary Examiner US. Cl. X.R.