Process for preparing potassium monoethyl malonate

Details Process for preparing potassium monoethyl malonate Process for preparing potassium monoethyl malonate

1999-04-19

2001-01-09

Lee, Howard C. (Department: 1623)

Organic compounds -- part of the class 532-570 series

Organic compounds

Carboxylic acid esters

C560S191000

Reexamination Certificate

active

06172257

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
The invention relates to a process for preparing potassium monoethyl malonate (or the potassium salt of malonic acid monoethyl ester; designated KEM hereafter) by selective saponification of diethyl malonate (or malonic acid diethyl ester; designated DEM hereafter) with potassium hydroxide, the target product being obtained in high purity.
2. Discussion of the Background
KEM is used as a precursor for the syntheses of pharmaceuticals having a quinolone structure. The use for syntheses in the pharmaceutical area, however, requires high product purity. In particular, a significant content of dipotassium malonate (designated DKM hereafter) is undesired.
A synthesis of potassium monoethyl malonate which was described as early as in the last century by van't Hoff (
Ber. Dtsch. Chem. Ges.
7, 1572) and which is still currently practiced starts from DEM which is selectively saponified with potassium hydroxide. According to EP 0 720 981 Al, this is performed using equimolar amounts of starting material in an alcoholic medium. However, the sought-after selective saponification is achieved only to an inadequate extent, so that only a target product considerably contaminated with dipotassium malonate (DKM) is obtained. The content of DKM is customarily in the order of magnitude of several % by weight. Removal of the dipotassium malonate from the potassium monoethyl malonate which is necessary for use of the latter as a pharmaceutical precursor is difficult and includes extensive purification operations. A further disadvantage of the known process is the relatively high dilution at which the process must be carried out. The alcohol is used at 19 to 28 times the amount by weight of potassium hydroxide. This large amount of alcohol has an adverse effect on the space-time yield and increases the expense for recovery of the solvent. In the case of the processes mentioned, the amount of alcohol is further increased by the DEM likewise being used in alcoholic solution.
Box et al.,
Heterocycles,
Vol. 32, No. 2, 1991, 245 ff., describe a synthesis of &bgr;-lactones and &bgr;-lactams, in which KEM is as intermediate. The two starting materials are, as in the process described in EP 0 720 981 Al discussed above, used in equimolar amounts, that is to say each at 100 mmol. The molar ratios of DEM to KOH were calculated incorrectly, however, since 20.225 g of DEM is 126 mmol and is equivalent to 1.26 times the molar amount, based on KOH. If it is further assumed that the potassium hydroxide used had, as is commercially usual, a KOH content of approximately 90% by weight (remainder water), 20.225 g of DEM are actually equivalent to 1.38 times the molar amount, based on KOH (calculated as 100%). Working using molar ratios of 1.26:1 and 1.38:1 showed that although pure KEM containing less than 0.5% by weight of DKM was obtainable by this process, the precipitated KEM was really difficult to filter. In the case of laboratory batches, the filtration time was more than two hours. Such times are prohibitive for production on an industrial scale. In addition, according to Box et al., similar to the process of EP 0720 981 Al cited above, considerable amounts of alcohol are required. Finally, the yields of KEM are not satisfactory either.
SUMMARY OF THE INVENTION
One of the objects of the present invention is to provide a process for preparing potassium monoethyl malonate which avoids the above disadvantages, i.e., gives high yields of a pure low-DKM and readily filterable KEM without the use of large amounts of alcohol.
This object, and others, is achieved by a process for preparing potassium monoethyl malonate by selective saponification of malonic acid diethyl ester with potassium hydroxide, in which the potassium hydroxide is added to the malonic acid diethyl ester, malonic acid diethyl ester and potassium hydroxide are used in a molar ratio of at least 1.5 and the potassium hydroxide is effectively distributed in the malonic acid diethyl ester.
A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description.
DETAILED DESCRIPTION OF THE INVENTION
The process according to the present invention provides potassium monoethyl malonate that may have a DKM content of <1% by weight (such as at most 0.1, 0.2, 0.3, 0.5, 0.8 or 1% by weight), as required for pharmaceutical syntheses, shows acceptable filtration times and requires a comparatively low energy consumption for recovery of the alcohol and of the excess malonic acid diethyl ester. The high purity of the KEM was surprising, since the measures according to the invention do not show a comparable effect in the case of the homologous malonic acid dimethyl ester (or dimethyl malonate; DMM). The Comparison Examples 2 and 3 show that DMM, even without the molar ratio of KOH to DEM according to the invention and even without effective distribution of the potassium hydroxide, gives a potassium monomethyl malonate (KMM) having low contents of DKM. In addition, it was surprising, and critical for production on an industrial scale, that the KEM according to the invention is very readily filterable, as can be seen from Comparison Example 6. This effect is difficult to explain, even with hindsight. Finally, it is surprising, that sodium monoethyl malonate (NaEM), analogous to the KEM, under the conditions according to the invention gives an NaEM having a high content of disodium malonate (DNaM), furthermore in poor yield, as Comparison Example 4 shows. In addition, there is the fact that the NaEM reaction mixture is considerably more difficult to filter than the corresponding KEM mixture in the present process according to the invention. Filtration of the first lasts approximately ten times as long, with correspondingly poorer space-time yield
An important feature of the process according to the invention is that the potassium hydroxide is added to the malonic acid diethyl ester which is therefore present in excess over the entire course of the reaction. The potassium hydroxide is advantageously used in the form of a solution in particular an alcoholic solution. In order to avoid transesterifications, preferably ethanol is used as the alcoholic solvent. For this purpose, the approximately 96 percent by weight ethanol can be used, as is produced as an azeotrope in the distillation of aqueous alcoholic mixtures. Alternatively, ethanol having other, similarly low, water contents can be used, or preferably the so-called absolute anhydrous alcohol can be used. The solution can contain other inert low-boiling solvents, such as aliphatic, cycloaliphatic or aromatic hydrocarbons, without particular advantage being associated therewith. In the solution, the alcohol and, if appropriate, other solvents, are generally present at 3 to 10 times, advantageously 4 to 8 times, the amount by weight, based on potassium hydroxide. These ranges include all specific values and subranges therebetween, such as 3.5, 4.5, 5, 6, 7 and 9 times the amount of potassium hydroxide. The process according to the invention therefore succeeds with less alcohol or solvent than the known processes described above.
Another important feature of the present process is the molar excess in which the malonic acid diethyl ester is used, more precisely advantageously without added solvent or diluent. At a molar ratio of 1.5 to 12 mol, preferably 2 to 8 mol, and in particular 3 to 5 mol, malonic acid diethyl ester per mole of potassium hydroxide, on the one hand the high product purity which is characteristic of the process according to the invention is achieved, and on the other hand the reaction mixture, despite the target product precipitating in crystalline form, is ensured to remain handleable as a suspension. These ranges for the molar ratio of malonic acid diethyl ester to potassium hydroxide including 2.5, 4, 4.5, 5.5, 6, 7, 9, 10 and 11 mol. The excess can be less, within the specified limits, if the amount

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