Process for the preparation of hydroxy methylthiobutyric...

Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acid esters

Reexamination Certificate

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C426S002000, C562S581000, C564S129000

Reexamination Certificate

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06479695

ABSTRACT:

The present invention relates to a process for the preparation of 2-hydroxy-4-methylthiobutyric acid esters and in particular to a two-stage process consisting of hydrating 2-hydroxy-4-methylthiobutyronitrile and then esterifying the intermediate product obtained.
2-Hydroxy-4-methylthiobutyric acid is known to be used as a methionine analogue for feeding breeding animals and mainly, among these animals, poultry. This product is marketed under the trademarks Rhodimet AT 88™ or Alimet™.
It is known to prepare 2-hydroxy-4-methylthiobutyric acid by various processes for hydrating 2-hydroxy-4-methylthiobutyronitrile. The hydrolysis is carried out with an inorganic acid such as hydrochloric or sulphuric acid or it can also be carried out by enzymatic hydrolysis.
The esters have been prepared from the commercially available acid by a process which consists of preparing the hydrochloride salt of the acid and then in reacting it with the alcohol.
It is also known to prepare the 2-hydroxy-4-methylthiobutyric acid esters by hydration of 2-hydroxy-4-methylthiobutyronitrile by sulphuric acid to produce the 2-hydroxy-4-methylthiobutyramide. The amide is then converted to the acid by further hydrolysis. The monomeric form of the acid may then isolated from the mixture of monomers, and oligomers and esterified to produce the ester.
We have found that the esters can be prepared from the nitrile which avoids the preparation of the acid, by utilising the same reaction medium for the hydrolysis step and the esterification step.
Accordingly, the present invention provides a process for the preparation of 2-hydroxy-4-methylthiobutyric acid esters which comprises (a) a first step of, reacting 2-hydroxy-4-methylthiobutyronitrile with sulphuric acid to produce 2-hydroxy-4-methylthiobutyramide, and (b) a second step of reacting the 2-hydroxy-4-methylthiobutyramide with an alcohol to produce a 2-hydroxy-4-methylthiobutyric acid esters, the two steps being carried out in the same reaction medium.
The present invention provides the advantage over the known prior art processes in that the ester can be prepared from the nitrile and amide, thus avoiding the preparation of the acid, the chlorination and the subsequent esterification steps as required in the prior art processes. In particular, the process of the present invention provides the advantage over the prior art by avoiding the preparation of the acid and thus the necessary separation step of the monomers from the oligomers is also avoided.
In general, the reaction medium of the two steps comprises sulphuric acid.
The first step of the process is the hydration of 2-hydroxy-4-methylthiobutyronitrile by the addition of sulphuric acid. It has been found that it is possible to carry out the hydration of 2-hydroxy-4-methylthiobutyronitrile to 2-hydroxy-4-methylthiobutyric acid ester with excellent yields when the process is carried out in a highly concentrated sulphuric acid medium and in the presence of a sufficient quantity of water to carry out this reaction. Suitably, the molar ratio of sulphuric acid to 2-hydroxy-4-methylthiobutyronitrile is from 0.6 to 1.2, preferably between 0.6 and 1 and most particularly between 0.6 and 0.88. The rate of the reaction is inversely proportional to the quantity of water. Thus, a quantity of water equal to at least one mole of water per mole of 2-hydroxy-4-methylthiobutyronitrile is necessary. Preferably, the molar quantity of water is from 1 to 3. A molar ratio of water to the 2-hydroxy-4-methylthiobutyronitrile of from 1 to 2.5 is most preferred. Preferably, the 2-hydroxy-4-methylthiobutyronitrile is present in an aqueous solution containing at least 80% 2-hydroxy-4-methylthiobutyronitrile.
This low concentration of water very greatly limits, during the first step, the successive hydrolysis of 2-hydroxy-4-methylthiobutyroamide to 2-hydroxy-4-methylthiobutyric acid. It is thus preferable, during this first step, not to produce more than 5%, preferably less than 2% by weight of 2-hydroxy-4-methylthiobutyric acid. It is also preferable, during this first step, to obtain a concentration of 2-hydroxy-4-methylthiobutyroamide greater than 95% by weight, preferably greater than 98% by weight.
The operating conditions used in the first step are chosen within limits which do not lead to the production of 2-hydroxy-4-methylthiobutyric acid; it is thus preferable to work at a temperature of less than 60° C. and in particular from 0 to 50° C. The reaction pressure is preferably chosen between 0.01 and 3 bar.
The reaction is preferably carried out in a continuous system of reactors in series with a residence time of between 15 minutes and 2 hours.
The second step of the reaction is an esterification and or concomitantly a hydrolysis and an esterification of the 2-hydroxy-4-methylthiobutyroamide to a 2-hydroxy-4-methylthiobutyric acid ester. The second step is carried out in the presence of the remaining quantity of sulphuric acid not consumed in the first step and in the presence of a sufficient quantity of alcohol to esterify the amide present. The molar ratio between the alcohol and the amide is preferably between 2 and 6 and most particularly between 2 and 4. The alcohol is suitably an aliphatic alcohol containing 1 to 10 carbon atoms. The alcohol may be linear or branched. The use of a branched alcohol and most particularly of isopropyl alcohol is preferred.
This second step may be carried out, at a temperature of between 60 and the boiling point of the alcohol and under a pressure of from 0.5 to 5 bar. A pressure below atmospheric pressure makes it possible to remove traces of foul-smelling light gases for example of the dimethyl sulphide, dimethyl disulphide and methyl mercaptan type. The small excess of acid and the presence of ammonium hydrogen sulphate greatly limit the corrosive power of the medium at this temperature.
The process of the present invention may be carried out on a industrial scale and a means of carrying out the invention industrially may be according to the following sequence of steps starting with a concentrated solution of 2-hydroxy-4-methylthiobutyronitrile. A concentrated solution of 2-hydroxy-4-methylthiobutyronitrile and a solution of concentrated sulphuric acid, containing less than 20% by weight of water, is used.
The concentrated 2-hydroxy-4-methylthiobutyronitrile at about 80% by weight and the concentrated sulphuric acid at about 90% by weight are fed to an apparatus in which the 2-hydroxy-4-methylthiobutyronitrile is hydrated. A solution containing 2-hydroxy-4-methylthiobutyramide and any unreacted sulphuric acid is thus obtained. The alcohol is added to this solution. The solution obtained after heating contains the 2-hydroxy-4-methylthiobutyric acid ester. The 2-hydroxy-4-methylthiobutyric acid ester is recovered from this solution.
This particular industrial process may be carried out continuously, semi-continuously or batchwise. When the process is carried out continuously, the apparatus used for the hydration of 2-hydroxy-4-methylthiobutyronitrile may comprise a first stirred reactor with an external recirculation loop which in particular serves to remove the heat released by the reaction. The hydration of the 2-hydroxy-4-methylthiobutyronitrile may be completed in one or more stirred or piston reactors, preferably in series with the first reactor. A solution containing 2-hydroxy-4-methylthiobutyramide is thus obtained.
The alcohol is added to the amide solution. The apparatus used for the hydrolysis/esterification or the esterification of the 2-hydroxy-4-methylthiobutyramide may comprise a first stirred reactor. The hydrolysis/esterification or the esterification of the 2-hydroxy-4-methylthiobutyramide may be completed according to a scheme for industrial implementation in one or more stirred or piston reactors in series with the first hydrolysis reactor.
The industrial process may equally be operated starting with concentrated 2-hydroxy-4-methylthiobutyronitrile at about 80% by weight, the alcohol and sulphuric acid. The concentrated 2-hydroxy-4-methylthiobutyronitrile at about 80% by

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