Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2002-05-02
2002-11-26
Rotman, Alan L. (Department: 1625)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
C546S249000, C546S250000, C546S344000
Reexamination Certificate
active
06486327
ABSTRACT:
Hydroxymethylpyridines are valuable intermediates and find use, for example, in the synthesis of pharmaceuticals and agrochemicals, such as mefloquine hydrochloride or pineprofen.
The literature already describes a multiplicity of highly varied process variants for their preparation.
Chem. Abstr. Vol. 127; 293140, Vol. 106; 18373 or Vol. 103; 215195 discloses that 2- or 4-hydroxypyridine can be prepared in a yield of about 81 to 87% by catalytic reduction of the corresponding 2-cyano-pyridine.
Disadvantages of this process are the required high pressure and in particular the high price of the starting material.
A further possibility is the catalytic reduction of pyridinealdehydes using H
2
over Ba-promoted Cu chromite catalysts at 180 to 230° C. according to Chem. Abstr. Vol. 103: 215198 or the reduction with NaBH
4
according to Chem. Abstr. Vol. 93: 71487, and the latter says that the reactivity of the aldehydes toward reduction decreases in the order 2,6-pyridinecarboxaldehyde, 6-methyl-2-pyridinecarboxaldehyde, 4-pyridinecarboxaldehyde, 2-pyridinecarboxaldehyde and 3-pyridinecarboxaldehyde.
The disadvantage of these catalytic hydrogenations is that, owing to the deactivation of the catalyst used in each case, a large proportion of aldehyde is left unconverted, so that the end product is contaminated by large quantities of aldehyde.
A further disadvantage is the poor availability of the pyridinealdehyde.
Examples of other known variants are electro-chemical reduction of picolinic esters (e.g.: EP-A1-0 189 678) or the oxidation of alpha-picoline N-oxides sing trifluoroacetic anhydride (e.g.: Chem. Abstr. Vol. 122: 239462).
It is an object of the present invention to provide a process for preparing hydroxymethylpyridines which starts from easily accessible starting compounds and ensures a high purity of the desired end products, while allowing for a simple removal of interfering by-products.
The invention accordingly provides a process for preparing hydroxymethylpyridines which comprises
a) subjecting the corresponding vinylpyridine to ozonolysis in an alcohol solvent and hydrogenating the resulting peroxidic solution in the presence of a hydrogenation catalyst,
b) adjusting the hydrogenation solution by addition of a base to a pH of from 10 to 14 and distilling off the alcohol, and then
c) isolating the desired hydroxymethylpyridine in high purity by extraction with an organic solvent and subsequent distillative purification.
The process of the invention provides hydroxymethylpyridines (HMPs) in high purity. The process is particularly suitable for preparing a multiplicity of hydroxymethylpyridines such as 2-, 3- or 4-hydroxymethylpyridine, 6-methyl-2-hydroxy-methylpyridine, 2,6-di(hydroxymethyl)pyridine, etc. According to the invention, 2-, 3- or 4-hydroxy-methylpyridine are preferably prepared, and 2-hydroxymethylpyridine is more preferably prepared.
The corresponding vinylpyridine serves as the starting compound, such as 2-, 3- or 4-vinylpyridine, 6-methyl-2-vinylpyridine and 2,6-divinylpyridine, which is converted in the first step by ozonolysis with subsequent catalytic hydrogenation.
The ozonolysis is carried out at temperatures of −80° C. to +20° C., preferably at −30° C. to +10° C. and more preferably at −25° C. to +5° C.
The corresponding vinylpyridine is reacted with maximally equivalent amount of ozone since the ozonolysis proceeds below the theoretical ozone consumption under the given process conditions. Stoichiometric quantities of the vinylpyridine used in each case are consumed. After the ozonization has ended, no measures are required to expel excess or unconverted ozone from the reaction mixture before hydrogenation.
The reaction with ozone takes place in an aliphatic C
1
-C
4
-alcohol, such as methanol, ethanol, butanol or propanol. Preferred solvents are methanol and ethanol, of which methanol is more preferred.
The catalytic hydrogenation of the ozonolysis products following the ozonization preferably takes place in highly dilute solution, the measure described below ensuring that during the entire hydrogenation a peroxide content of maximum 0.1 mol/l, preferably of maximum 0.05 mol/l and in particular of maximum 0.02 mol/l is set and maintained. To this end, a hydrogenation reactor is charged with a suspension of the catalyst in the alcoholic solvent used during ozonolysis and the solution resulting from the ozonization is continuously fed in by means of an adjustable metering apparatus. While the ozonization solution is added at the beginning and in the course of the hydrogenation care must of course be taken that the peroxide content in the hydrogenation reactor specified above not be exceeded owing to the introduced amount of the peroxidic ozonolysis products.
As a result of the low concentration of peroxidic ozonolysis solution in the reaction medium during the actual hydrogenation process caused by the continuous feeding in, a rapid reduction is ensured. In this way, poisoning of the catalyst and the loss of activity associated with it is prevented. Viewed overall, the continuous addition moreover allows a large quantity of ozonolysis products to be reduced in a comparatively small volume, which results in high concentrations of the corresponding HMP and savings in time and also in the costs of the distillative removal of the solvent.
Useful catalysts for the hydrogenations are suitable noble metal catalysts, which may be used in the form of powder catalysts with support materials or without support material. Palladium or platinum catalysts are preferably used. Examples of suitable support materials for powder catalysts include carbon, aluminum, silica gel or kieselguhr. Although yields are independent of the catalyst quantity used, in order to attain a sufficient hydrogenation rate it is recommended to use an initial charge of the catalysts mentioned in noble metal quantities of from 0.1 to 20% by weight, preferably from 1 to 15% by weight and more preferably from 5 to 10% by weight, based in each case on the total quantity of the ozonized vinylpyridines fed in per hour.
After the reduction has ended, the catalyst is separated from the reaction mixture.
In the process of the invention, equivalent quantities of hydrogen are consumed in reducing the ozonolysis products. The quantity of hydrogen which can be used in the hydrogenation ranges from one mole equivalent to a multiple molar excess. From 1.3 to 2.5 mol equivalents of hydrogen are preferably used, and from 1.8 to 2.2 mol equivalents are more preferably used.
The hydrogenation advantageously takes place under virtually atmospheric conditions. Virtually atmospheric conditions are to be understood as meaning pressures of from 1 to about 3 bar, as is customary in industrial practice to prevent ingress of air into the hydrogenation reactor. In this way, the reduction of the ozonolysis products is very simple to practice in industry. However, it is also possible to perform the hydrogenation under a pressure of up to 20 bar and thereby increase the rate of hydrogenation. The reduction is exothermic and in a preferred embodiment is conducted at temperatures of from 20 to 60° C., in particular at temperatures in the range from 35 to 50° C.
After the hydrogenation, the reaction solution is separated from the catalyst and preferably concentrated, for example using a rotary evaporator, and the alcohol used as solvent is distilled off as an alcohol-water mixture. The formaldehyde formed as a by-product of the conversion of the vinylpyridines to the corresponding HMP is also removed substantially from the reaction solution. In order to recycle the alcohol, formaldehyde can be converted, for example by means of an acidic ion exchanger to formaldehyde dialkyl acetal, separated distillatively from the alcohol and then burnt.
After the concentration, the remaining reaction solution is then admixed with a suitable base, such as NaOH, KOH, CaOH, etc., and preferably with NaOH in combination with aqueous ammonia, preferably in 25% strength, so that a pH value of from 10 to 14,
Giselbrecht Karlheinz
Hermanseder Rudolf
Coppins Janet L
DSM Fine Chemicals Austria Nfg GmbH & Co KG
Rotman Alan L.
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