ZA200601864B

ZA200601864B - Process for purifying mesotrione

Info

Publication number: ZA200601864B
Application number: ZA200601864A
Authority: ZA
Inventors: Wichert Julie Marie; Guidetti-Grept Regine Laure; Benke Alan Henry
Original assignee: Syngenta Participations Ag
Priority date: 2003-10-02
Filing date: 2006-03-03
Publication date: 2007-07-25
Also published as: GB0323090D0; CN1860102A; CN100378071C; GT200400195A; UA82722C2

Description

PROCESS POR PURIFYING MESOTRIONE

The present invention relates to a novel process for reducing the level of impurities in a mesotrione sample.

Mesotrione (22 -nitro-4’-methylsulphonyl benzoyl)-1,3-cyclohexanedione) isa selective com herbicide and has the structure of formula (I) 0 0] NO, oO SO,CH,

Mesotrione is prepared by reacting 2-nitro-4-methylsulphonyl benzoyl chloride with cyclohexanedione to give the enol ester, followed by a rearrangement reaction to give mesotrione, as shown in the following reaction scheme:

OCI

NO, + + (CHCH)N Solvent

SO,CH, ° 0]

NO, O HO 1% 8 : H,C>—CN 0] HC

TT CHO o o CHO: er 2-Nitro-4-methylsulphonyl benzoyl chloride (NMSBC) is prepared from the corresponding 2-nitro-4-methylsulphonyl benzoic acid (NMSBA), which in turn is prepared by oxidation of 2-nitro-4-methylsulphonyl toluene (NMST). More details on the preparative route may be found in US4695673.

However, we have found that this process generally results in undesirable level of impurities being present in the final mesotrione product. One method we have found of reducing the impurities is to subject the NMSBA to a purification process before converting to NMSBC, as described in more detail in W002/076934. However, purifying the NMSBA does not always guarantee that the final product is free from, or has sufficiently low levels of, these impurities.

It is therefore an object of the present invention to provide an improved process for reducing the level of impurities in a mesotrione sample.

Accordingly, the present invention provides a process for reducing the levels of impurities in a mesotrione sample, said process comprising the steps of: @) forming a mesotrione enolate solution in an aqueous solvent, (ii) carmying out one or more purification processes, and (iii) crystallising the purified mesotrione out of solution.

Optionally, the process may further comprise a distillation step, which is suitably carried out prior to forming the mesotrione enolate. Generally, the distillation step will only, although not necessarily, be used if the mesotrione product has not been isolated after its preparation.

The enolate solution may be formed by the addition of an appropriate base, for example NaOH, KOH, NH,OH, pyridine or triethylamine; suitably the enolate is formed by the addition of NaOH or KOH. Suitably, the aqueous solvent is water, although in some cases an additional solvent, for example acetonitrile, methanol, ethanol, acetone, dimethylformamide etc, may be required to ensure complete dissolution of the mesotrione enolate. The mesotrione enolate solution is suitably formed at a pH of 6-13.

The one or more purification processes may be selected from the following: (a) filtration, (b) adsorption with suitable sorbent, such as carbon, clay etc., (c) extraction with an organic solvent, or (d) decantation.

Any number of the purification processes may be carried out and they may be performed in any order. Suitably, at least two purification processes are carried out and preferably at least three. The purification processes will now be described in further detail.

Filtration is carried out to remove any insoluble impurities that remain in the mesotrione enolate solution. The filtration may be carried out by any suitable method known in the art to a skilled person.

Adsorption treatment adsorbs impurities from the mesotrione enolate solution. A mesotrione enolate solution of suitably 1-30%, and preferably 8-11% is contacted with carbon in a batch or continuous fashion for a period of several hours. Concentration of the adsorbent solution relative to the concentration of mesotrione in the enolate is suitably 2- 40% and preferably 10-20%. The pH for adsorption treatment is suitably between pH 5 and 13, and preferably between pH 9 and 11.

Extraction with an organic solvent is carried out to remove any impurities, which are soluble in the organic phase but insoluble in the aqueous phase. An organic solvent is added to the mesotrione enolate aqueous solution and some impurities will preferentially dissolve in the organic phase which is then removed and discarded. The mesotrione enolate aqueous solution may be ‘washed’ a number of times with organic solvent, such as once, twice, three times, four times etc or continuously contacted in a counter current column. It is unlikely that more than four ‘washings’ would be required as all the impurities soluble in the organic solvent are likely to have been removed after this number of ‘washings’. Suitable organic solvents will be known to those skilled in the art, but may include benzonitrile, acetonitrile/xylene, xylene, methylene chloride, MIBK, ethyl ether, n-hexane and 1,2- dichloroethane.

Decantation simply refers to the removal of any organic solvent from the solution.

Organic solvent is likely to remain with the mesotrione enolate aqueous solution if the mesotrione product has not been isolated after its preparation and no distillation step is carried out. Removal of the organic solvent will remove any impurities soluble in the organic solvent, but insoluble in the aqueous solution.

The optional distillation step is suitably carried out prior to forming the mesotrione enolate solution and will remove any organic solvent remaining after the condensation/rearrangement reaction described above.

The crystallisation step may be carried out by any method known to those skilled in the art. For example, the process may be a batch method, a semi-batch method or a- continuous crystallisation method. The crystallisation is suitably effected by reducing the pH of the mesotrione enolate solution, for example by the controlled addition of acid such as hydrochloric acid. Seed crystals of mesotrione may be used to assist the crystallisation process. Optionally, a water-soluble solvent may be added, since the presence of a water soluble solvent such as acetonitrile aids in reducing the amount of impurities present at this point. _

In one specific embodiment of the invention, the process comprises: a distillation step; formation of a mesotrione enolate solution, preferably the potassium enolate; one or more purification steps; and crystallisation of mesotrione.

In a second specific embodiment of the invention, the process comprises: formation of a mesotrione enolate solution, preferably the potassium enolate; decantation, filtration and adsorption treatment, carried out in any order (although preferably the decantation process is carried out first); and crystallisation of mesotrione.

By carrying out the process according to the invention, the level of impurities in the final mesotrione product is reduced to an acceptable level.

A further advantage of the process of the present invention is that is can be integrated into the mesotrione manufacturing process, thus eliminating the need for isolation of crude mesotrione followed by purification. Accordingly, a further aspect of the invention provides an integrated manufacturing/purification process for mesotrione, said process comprising the steps of: @) reacting cyclohexanedione with 2-nitro-4-methylsulphonyl benzoyl! chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; (ii) formation of mesotrione enolate in aqueous solution; (ili) carrying out one or more purification processes, and (iv) crystallising the purified mesotrione ouit of solution.

Optionally, the process may further comprise a distillation step, which is suitably carried out prior to forming the mesotrione enolate.

Optionally, the NMSBC is first subjected to a carbon purification treatment.

Thus, one specific embodiment of this aspect of the invention provides an integrated manufacturing/purification process for mesotrione, said process comprising: reacting cyclohexanedione with 2-nitro-4-methylsulphonyl benzoyl chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; a distillation step;

formation of potassium enolate mesotrione solution; one or more purification steps; and crystallisation of mesotrione.

A second specific embodiment of this aspect of the invention provides an integrated manufacturing/purification process for mesotrione, said process comprising reacting 5 cyclohexanedione with 2-nitro-4-methylsulphonyl benzoyl chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; formation of a mesotrione enolate solution, preferably the potassium enolate; decantation, filtration and adsorption treatment, carried out in any order (although preferably the decantation process is carried out first); and crystallisation of mesotrione.

Previously, in order to attempt to obtain a final mesotrione product with an acceptable level of impurities, it was necessary to subject the crude NMSBA (prepared by oxidation of NMST) to a purification process, as described in W002/076934. However, as "mentioned above, this did not always give sufficiently low levels of impurities in the final mesotrione product to be acceptable. Surprisingly, we have now found that if the process of the invention is followed, the purification of NMSBA is not essential or at most only ‘partial’ purification, such as one step as opposed to the two or three disclosed in

W002/076934, is required; that is acceptable levels of impurities can be obtained in the final mesotrione product when less purified or even crude NMSBA is used. Accordingly, a yet further aspect of the invention provides a process for preparing mesotrione, said method comprising: @) Oxidation of NMST to give crude NMSBA; (ii) conversion of NMSBA to NMSBC; (iii) reacting cyclohexanedione with 2-nitro-4-methylsulphonyl benzoyl chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; (iv) formation of mesotrione enolate in aqueous solution; (v) carrying out one or more purification processes, and (vi) crystallising the purified mesotrione out of solution.

Optionally, the process may further comprise partial purification of crude NMSBA.

Thus one specific embodiment of this aspect of the invention provides a process for preparing mesotrione, said process comprising: oxidation of NMST to give crade NMSBA; optional partial purification of crude NMSBA; conversion of NMSBA to NMSBC; reacting cyclohexanedione with 2._nitro-4-methylsulphonyl benzoyl chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; 8 distillation step; formation of mesotrione enolate solution, preferably the potassium enolate; one or more purification steps; and crystallisation of mesotrione.

A second embodiment of this aspect of the invention provides a process for preparing mesotrione, said process comprising: oxidation of NMST to give crude NMSBA,; optional partial purification of crude NMSBA; conversion of NMSBA to NMSBC; reacting cyclohexanedione with 2-nitro-4-methylisulphonyl benzoyl chloride NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; formation of a mesotrione enolate solution; decantation, filtration and adsorption treatment carried out in any order; and crystallisation of mesotrione.

The present invention will now be described further by way of example only.

Example 1

This is an example of the solid adsorption treatment (using carbon as adsorbent) of previously isolated mesotrione which had high levels of impurities. The additional purification option of pre-filtration was used in these examples.

Example | Treatment Original | Impurities | %

No. Impurities | Content Reduction

Content after in

PPM) Treatment | Impurities

PP Content 1A Already isolated mesotrione was dissolved | 7900 2800 65% into a 10 % enolate solution at pH 9.5 with

KOH. The mixture was pre-filtered and contacted with 15 % carbon for 2.5 hours before being filtered and batch crystallized following standard lab procedures. 1B Already isolated mesotrione was dissolved | 7400 4500 39% into a 10 % enolate solution at pH 9.5 with

KOH. The mixture was pre-filtered and contacted with 15 % carbon for 2.5 hours before being filtered and batch crystallized following standard lab procedures. 1C Already isolated mesotrione was dissolved | 7400 69 % into a 10 % enolate solution at pH 9.5 with

NaOH/acetonitrile. The enolate was pre- filtered and contacted with 15 % carbon for 2.5 hours before being filtered and batch crystallized following standard lab procedures. iD Already isolated mesotrione was dissolved | 8800 78 % into a 10 % enolate solution at pH 9.5 with

NaOH/acetonitrile. The enolate was pre- filtered and batch carbon treated with 9 % carbon for 3 hours. The carbon was filtered and the enolate was crystallized in a continuous reactor following standard lab 1E Already isolated mesotrione was dissolved | 8800 3100 65% into a 10 % enolate solution at pH 9.5 with triethylamine. The enolate was pre-filtered and batch carbon treated with 9 % carbon for 3 hours. The carbon was filtered and : the enolate was crystallized in a continuous reactor following standard lab procedures.

IF Already isolated mesotrione was dissolved 7900 4600 42% into a 10 % enolate solution at pH 9.5 with

NaOH/acetonitrile. The mixture was pre- filtered and contacted with 15 % carbon for 2.5 hours before being filtered and batch crystallized following standard lab procedures. 1G Already isolated mesotrione was dissolved | 7400 38% into a 10 % enolate solution at pH 9.5 with :

NaOH. The mixture was pre-filtered and contacted with 15 % carbon for 2.5 hours before being filtered and batch crystallized following standard lab procedures.

Example 2

This is an example of a solvent extraction treatment of previously isolated mesotrione which had high levels of impurities.

Example | Treatment Original | Impurities | %

No. Impurities | Content | Reduction

Content after in (PPM) Treatment | Impurities

PP Content 2A Already isolated mesotrione was dissolved | 8000 49 % into a 10 % enolate solution at pH 12.5 with KOH. The mixture was contacted with 1,2-dichloroethane, the 1,2- dichloroethane was extracted, and the remaining aqueous layer was batch crystallized following standard lab

DIrocCedures.

Already isolated mesotrione was dissolved | 8000 46 % into a 10 % enolate solution at pH 12.5 with KOH. The mixture was contacted with benzonitrile, the benzonitrile was extracted, and the remaining aqueous layer was batch crystallized following standard lab procedures.

Example 3

This is an example of an integrated adsorption treatment of in-process mesotrione enolate. NMSBA purified by standard procedures was used as the starting material. The mixture was distilled before the enolate treatments and the purification element of pre- filtration was included. Different adsorbent loadings are shown in the examples in this table.

Example | Treatment Original | Impurities | %

No. Impurities { Content Reduction

Content after in (PPM) Treatment | Impurities

PP! Content 3A Mesotrione was made using the standard 13800 20% process from NMSBA purified by standard procedures. After the distillation, an enolate solution at pH 9.5 was formed with

KOH. The mixture was pre-filtered and contacted with 13 % carbon for 2 hours before being filtered and batch crystallized following standard lab procedures.

3B Mesotrione was made using the standard 13800 63 % process from NMSBA purified by standard procedures. After the distillation, an. enolate solution at pH 9.5 was formed with

KOH. The mixture was pre-filtered and contacted with 27 % carbon for 3.5 hours before being filtered and batch crystallized following standard lab procedures. . 3C Mesotrione was made using the standard 13800 5700 59% : process from NMSBA purified by standard procedures. After the distillation, an enolate solution at pH 9.5 was formed with :

KOH. The mixture was pre-filtered and contacted with 40 % carbon for 2 hours before being filtered and batch crystallized following standard lab procedures.

Mesotrionc was made using the standard 13800 5800 58% process from NMSBA purified by standard procedures. After the distillation, an enolate solution at pH 9.5 was formed with

KOH. The mixture was pre-filtered and contacted with 53 % carbon for 2 hours before being filtered and batch crystallized following standard lab procedures.

Mesotrione was made using the standard 17900 15900 11% process from NMSBA purified by standard procedures. After the distillation, an enolate solution at pH 9.5 was formed with

KOH. The mixture was pre-filtered and contacted with 5 % carbon for 2 hours : before being filtered and batch crystallized following standard lab procedures. 3F Mesotrione was made using the standard 17900 15000 16 % process from NMSBA purified by standard procedures. After the distillation, an "| enolate solution at pH 9.5 was formed with

KOH. The mixture was pre-filtered and contacted with 10 % carbon for 2 hours before being filtered and batch crystallized ‘ following standard lab procedures. 3G Mesotrione was made using the standard 17900 12300 31% process from NMSBA purified by standard procedures. After the distillation, an enolate solution at pH 9.5 was formed with

KOH. The mixture was pre-filtered and contacted with 20 % carbon for 2 hours before being filtered and batch crystallized following standard lab procedures.

Example 4

This is an example of an integrated adsorption treatment of in process mesotrione enolate. NMSBA purified by standard procedures was used as the starting material. The s mixture was distilled before the enolate treatment, and the purification element of pre- filtration was included. Different filtration conditions are used in the examples in this table.

Example | Treatment Original | Impurities | %

Noe. Impurities: | Content Reduction

Content after in (PPM) Treatment | Impurities

PP Content 4A Mesotrione was made using the standard 15800 7400 53% process from NMSBA purified by standard procedures. After the distillation, an enolate solution at pH 7 was formed with

KOH. The mixture was pre-filtered and : contacted with 10 % carbon for 2 hours before being filtered and batch crystallized following standard lab procedures. 4B Mesotrione was made using the standard 15800 7700 51% process from NMSBA purified by standard procedures. After the distillation, an enolate solution at pH 7 was formed with

KOH. The mixture was pre-filtered and contacted with 10 % carbon for 2 hours before being filtered and batch crystallized following standard lab procedures. 4C Mesotrione was made using the standard 15800 10400 34% - process from NMSBA purified by standard procedures. After the distillation, an enolate solution at pH 9.5 was formed with ‘| KOH. The mixture was pre-filtered and contacted with 10 % carbon for 2 hours before being filtered and batch crystallized following standard lab procedures.

Mesotrione was made using the standard 15800 8600 46 % process from NMSBA purified by standard procedures. After the distillation, an i enolate solution at pH 9.5 was formed with

KOH. The mixture was pre-filtered and contacted with 10 % carbon for 2 hours before being filtered and batch crystallized following standard lab procedures.

Example 5

This is an example of an integrated solvent extraction treatment of in process mesotrione enolate. Crude NMSBA was used as the starting material. The mixture was distilled before the enolate treatment.

Table 5

Example | Treatment Original | Impurities | %

No. Impurities | Content Reduction

Content after in

PPM) Treatment | Impurities

PP Content 5A Mesotrione was made using the standard 7800 29% process from crude NMSBA. After the distillation, an enolate solution at pH 13 was formed with KOH. The mixture was contacted with 1,2-dichloroethane, the 1,2- dichloroethane was extracted, and the : remaining aqueous layer was batch crystallized following standard lab procedures.

Example 6 ~ This is an example of an integrated adsorption treatment of in process mesotrione enolate. Partially purified NMSBA was used as the starting material. The mixture was distilled before the enolate treatment.

Table 6

Example | Treatment Original | Impurities | %

No. Impurities | Content | Reduction

Content after in (PPM) Treatment | Impurities

PP Content 6A Mesotrione was made using the standard 13300 6300 53% process from partially purified NMSBA .

After the distillation, an enolate solution at pH 5 was formed with NaOH and ACN.

The mixture was contacted with 20 % carbon for 2 hours before being filtered and batch crystallized following standard lab nrocedures.

Mesotrione was made using the standard 8500 4900 42% process from partially purified NMSBA(.

After the distillation, an enolate solution at pH 9 was formed with NaOH and ACN. :

The mixture was contacted with 20 % : carbon for 2 hours before being filtered and batch crystallized following standard lab procedures.

Example 7

This is an example of an integrated column adsorption treatment of in process mesotrione enolate. Crude NMSBA was used as the starting material. The mixture was distilled before the enolate treatment.

Example | Treatment Original | Impurities | %

No. Impurities | Content Reduction

Content after in (PPM) Treatment | Impurities

PP Content

TA Mesotrione was made from crude NMSBA 10500 8% following standard lab procedures. After the distillation, an enolate solution at pH 9.5 was formed with KOH. The mixture was pre-filtered and sent through a carbon column such that there was 14.9 % carbon usage. Samples were batch crystallized following standard lab procedures.

Mesotrione was made from crude NMSBA | 11400 11% following standard lab procedures. After the distillation, an enolate solution at pH 9.5 was formed with KOH. The mixture was pre-filtered and sent through a carbon column such that there was 5.08 % carbon usage. Samples were batch crystallized following standard lab procedures. 7C Mesotrione was made from crude NMSBA 6600 42% following standard lab procedures. After the distillation, an enolate solution at pH

9.5 was formed with KOH. The mixture was pre-filtered and sent through a carbon column such that there was 2.93 % carbon usage. Samples were batch crystallized following standard lab procedures.

Example 8

This is an example of an integrated adsorption treatment of in process mesotrione enolate. Purified or crude NMSBA was used as the starting material. TEA decantation is . included as a purification element. The mixture was distilled before the enolate treatment.

Example | Treatment Original | Impurities | %

No. Impurities | Content Reduction

Content after in (PPM) Treatment | Impurities : PP Content 8A Mesotrione was made from crude NMSBA | 51% by the standard process . An enolate solution at pH 13 was formed with KOH.

The TEA was decanted, and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab procedures. 8B Mesotrione was made from crude NMSBA | 20600 8900 57% by the standard process. After the distillation, an enolate solution at pH 13 was formed with KOH. The TEA was decanted, and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab procedures. 8C Mesotrione was made from crude NMSBA { 15000 6300 58% by the standard process. After the distillation, an enolate solution at pH 13 was formed with KOH. The TEA was decanted, and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab procedures.

NMSBA by the standard process . An enolate solution at pH 13 was formed with

KOH. The TEA was decanted, and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab procedures.

Mesotrione was made from purified 7300 60%

NMSBA by the standard process . An enolate solution at pH 13 was formed with

KOH after the completion of the solvent distillation. The TEA was decanted, and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab procedures.

Mesotrione was made from purified 6600 3300 50%

NMSBA by the standard process . An enolate solution at pH 13 was formed with

KOH after the completion of the solvent distillation. The TEA was decanted, and . the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab procequres.-

Example 9

This is an example of the effect of the presence of acetonitrile during crystallization on the impurity content of mesotrione. An integrated purification was done which used the purification elements of TEA decant and the presence of acetonitrile during the crystallization. The mixture was distilled before the enolate treatment. Crude NMSBA was used as the starting material.

Example | Treatment Original | Impurities | %

No. Impurities | Content Reduction

Content after in ‘ (PPM) Treatment | Impurities

PP Content 9A Mesotrione was made from crude NMSBA | 21800 12800 41% using the standard process. After solvent pH 13 was made and the TEA was decanted. The enolate was batch crystallized following standard lab procedures except that acetonitrile was present during the crystallization.

Mesotrione was made from crude NMSBA | 21800 12800 41% using the standard process. After solvent distillation, a potassium enolate solution at pH 13 was made and the TEA was decanted. The enolate was batch crystallized following standard lab procedures except that acetonitrile was present during the crystallization. 9C Mesotrione was made from crude NMSBA | 30900 9000 71% using the standard process. After solvent distillation, a potassium enolate solution at pH 13 was made and the TEA was decanted. The enolate was batch crystallized following standard lab procedures except that acetonitrile was present during the crystallization.

Example 10 :

This is an example of the integrated process starting with crude NMSBA in which a partial NMSBA purification is incorporated directly into the process. The purification elements of decantation and adsorption treatment are used in these examples.

Example | Treatment Original Impurities | %

No. Impurities | Content Reduction

Content after in (PPM) Treatment | Impurities

PP Content 10A Mesotrione was made from the integrated | 2900 2500 - 53% : process starting with crude NMSBA in water which was partially purified and distilled to remove water. Benzonitrile was added to make a NMSBA solution and the remaining water was distilled. Inorganic salts were filtered from the acid chloride after excess phosgene removal. The C/R : proceeded by normal reaction conditions.

An enolate solution at pH 13 was formed with KOH. The TEA and benzonitrile :

were decanted and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab procedures.

Mesotrionc was made from the integrated | 2900 62% process starting with crude NMSBA in water which was partially purified and distilled to remove water. Benzonitrile was added to make a NMSBA solution and the : remaining water was distilled. Inorganic salts were filtered from the acid chloride after excess phosgene removal. The C/R proceeded by normal reaction conditions.

An enolate solution at pH 13 was formed with KOH. The TEA and benzonitrile were decanted and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab 10C Mesotrione was made from the integrated | 2900 2100 28% process starting with crude NMSBA in water which was partially purified and distilled to remove water. Benzonitrile was added to make a NMSBA solution and the remaining water was distilled. Inorganic salts were filtered from the acid chloride after excess phosgene removal. The C/R proceeded by normal reaction conditions.

An enolate solution at pH 13 was formed with KOH. The TEA and benzonitrile were decanted and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab procedures.

Mesotrione was made from the integrated 1600 45% process starting with crude NMSBA in water which was partially purified and distilled to remove water. Benzonitrile was added to make a NMSBA solution and the remaining water was distilled. Inorganic salts were filtered from the acid chloride after excess phosgene removal. The C/R proceeded by normal reaction conditions.

An enolate solution at pH 13 was formed with KOH. The TEA and benzonitrile were decanted and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab procequres. ‘Mesotrione was made from the integrated | 2900 34% process starting with crude NMSBA in water which was partially purified and distilled to remove water . Benzonitrile was added to make a NMSBA solution and the remaining water was distilled. .

Inorganic salts were filtered from the acid chloride after excess phosgene removal.

The C/R proceeded by normal reaction conditions. An enolate solution at pH 13 was formed with KOH. The TEA and benzonitrile were decanted and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and ‘batch crystallized following standard lab procedures. 10F Mesotrione was made from the integrated | 2900 1500 48 % process starting with crude NMSBA in water which was partially purified and distilled to remove water at pH 0.8.

Benzonitrile was added to make a 20 %

NMSBA solution and the remaining water was distilled. Inorganic salts were filtered from the acid chloride after excess phosgene removal. The C/R proceeded by normal reaction conditions. An enolate solution at pH 13 was formed with KOH. :

The TEA and benzonitrile were decanted and the enolate was contacted with 20 % : carbon for 2 hours at pH 13 before being filtered and batch crystallized following standard lab procedures. 10G Mesotrione was made from the integrated | 4900 3100 37% process starting with crude NMSBA in water which was partially purified and distilled to remove water . Benzonitrile was added to make a NMSBA solution and the remaining water was distilled.

The C/R proceeded by normal reaction conditions. An enolate solution at pH 13 was formed with KOH. The TEA and benzonitrile were decanted and the enolate was contacted with 20 % carbon for 2 hours at pH 9.5 before being filtered and batch crystallized following standard lab

D rocedures. .

Mesotrione was made from the integrated 2500 22% process starting with crude NMSBA in water which was partially purified and distilled to remove water. Benzonitrile was added to make NMSBA solution and the remaining water was distilled. organic salts were filtered from the acid chloride after excess phosgene removal. The C/R proceeded by normal reaction conditions.

An enolate solution at pH 13 was formed with KOH. The TEA and benzonitrile were decanted and the enolate was contacted with 20 % carbon for 2 hours at : pH 9.5 before being filtered and batch crystallized following standard lab procedures.

Mesotrione was made from the integrated | 3200 38% process starting with crude NMSBA in water which was partially purified and distilled to remove water. Benzonitrile was added to make a NMSBA solution and the remaining water was distilled. Inorganic salts were filtered from the acid chloride after excess phosgene removal. The C/R proceeded by normal reaction conditions.

Example 11

Previously isolated mesotrione, made from crude NMSBA, was dissolved by addition of dilute potassium hydroxide to form a 9.1% w/w solution of potassium enolate at pHs 7,9.5 and 11, respectively. The very small amount of residual solid was removed by filtration.

Extraction

The aqueous solution of potassium enolate of mesotrione (183g) was extracted with solvent (150m) four times. The phases were separated after each extraction and the solvent phase was discarded. After the fourth extraction, the mesotrione was recovered from the aqueous phase by continuous crystallisation according to standard procedure. Analysis showed reduction of the impurities (Table 11A). The figures in parenthesis are the percentage of the impurities remaining after treatment. soe

Ter | eos | Awe

Adsorption

The aqueous solution of potassium enolate of mesotrione (183g) was stirred with 5g adsorbent at ambient temperature (~25°C) for 30 minutes. The adsorbent was removed by filtration and the mesotrione was recovered from the aqueous phase by continuous crystallisation according to standard procedure. Analysis showed reduction of the impurities (Table 11B). The figures in parenthesis are the percentage of the impurities remaining after treatment.

oo

Table 11B

Sum of impurities in mesotrione sample (%)

Ambersorb 348F 5.627 0.383 (6.81%) | 0.680 (12.1%) | 0.171 (3.04%)

Amberlite XAD4 -5.627 0.892 (15.9%) | 1.692 (30.1%)

Amberlite XAD16 0.245 (7.17%) | 0.063 (1.84%) | 0.145 (4.24%)

Molecular sieves SA 5.627 1.414 (25.1%) ] 1.792 (31.8%)

Claims

1. A process for reducing the levels of undesirable impurities in a mesotrione sample, said process comprising the steps of: @) forming a mesotrione enolate solution in an aqueous solvent, : (if) carrying out one or more purification processes, and (iii) crystallising the purified mesotrione out of solution.

2. A process according to claim 1, wherein the process further comprises a distillation step.

3. A process according to claim 1 or 2, wherein the one or more purification processes are selected from the group consisting of filtration, adsorption treatment, extraction with an organic solvent, and decantation.

4. A process for reducing the levels of undesirable impurities in a mesotrione sample, said process comprising: a distillation step, formation of a mesotrione enolate ‘ solution; one or more purification steps; and crystallisation of mesotrione.

5. A process for reducing the levels of undesirable impurities in a mesotrione sample, said process comprising: formation of a mesotrione enolate solution; decantation, filtration and adsorption treatment carried out in any order; and crystallisation of mesotrione.

6. An integrated manufacturing/purification process for mesotrione, said process comprising the steps of: (i) reacting cyclohexanedione with 2-nitro-4-methylsulphonyl benzoyl chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; (ii) formation of mesotrione enolate in aqueous solution;

(iif) carrying out one or more purification processes, and (iv) crystallising the purified mesotrione out of solution.

7. A process according to claim 6, wherein said process further comprises a distillation step.

8. A process according to claim 6 or 7, wherein the NMSBC is first subjected to a carbon purification treatment.

09. An integrated manufacturing/purification process for mesotrione, said process comprising: reacting cyclohexanedione with 2-nitro-4-methylsulpbonyl benzoyl chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; a distillation step; formation of a mesotrione enolate solution; one or more purification steps; and crystallisation of mesotrione.

10. An integrated manufacturing/purification process for mesotrione, said process comprising reacting cyclohexanedione with 2-nitro-4-methylsulphonyl benzoyl chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; formation of a mesotrione enolate solution; decantation, filtration and adsorption treatment, carried out in any order; and crystallisation of mesotrione.

11. A process for preparing mesotrione, said method comprising: i) Oxidation of NMST to give crude NMSBA; (ii) conversion of NMSBA to NMSBC; (iii) reacting cyclohexanedione with 2-nitro-4-methylsulphonyl benzoyl chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; (iv) formation of mesotrione enolate in aqueous solution; (v) carrying out one or more purification processes, and (vi) crystallising the purified mesotrione out of solution.

12. The method of claim 11, wherein the process further comprises partial purification of the crude NMSBA.

13. The method of claim 11 or 12, wherein the process further comprises a distillation step.

14. A process for preparing mesotrione, said process comprising: oxidation of NMST to give crude NMSBA;; optional partial purification of crude NMSBA; conversion of NMSBA to NMSBC; reacting cyclohexanedione with 2-nitro-4-methylsulphonyl benzoyl chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; a distillation step; formation of potassium enolate mesotrione solution; one or more purification steps; and crystallisation of mesotrione.

15. A process for preparing mesotrione, said process comprising: oxidation of NMST to give crude NMSBA,; optional partial purification of crude NMSBA; conversion of NMSBA to NMSBC; reacting cyclohexanedione with 2-nitro-4-methylsulphonyl benzoyl chloride (NMSBC) to form an enol ester followed by a rearrangement process to give mesotrione; formation of a mesotrione enolate solution; decantation, filtration and adsorption treatment carried out in any order; and crystallisation of mesotrione.