Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
1999-08-11
2001-01-16
Shah, Mukund J. (Department: 1624)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
active
06175019
ABSTRACT:
Process for the preparation of 1,3-dimethylimidazolium 4-carboxylate
The present invention relates to a process for the preparation of 1,3-dimethylimidazolium 4-carboxylate.
1,3-dimethylimidazolium 4-carboxylate is used, according to the parallel German Application No. 198 364 74.1, as catalyst in the preparation of isophoronenitrile (IPN) from isophorone and hydrogen cyanide.
1,3-dimethylimidazolium 4-carboxylate, a betaine of the formula I
is a natural substance and is known under the name norzooanemonin, the isolation and characterization of which has been described in Tetrahedron Lett. 38, (1997) 3883-4.
In Tetrahedron 29, (1973) 3135-6, 1,3-dimethylimidazolium 4-carboxylate is prepared by reacting imidazole-4-carboxylic acid with dimethyl sulfate. A disadvantage of this process is the requisite handling of the highly toxic dimethyl sulfate.
It is an object of the present invention to find an alternative economical process for the preparation of 1, 3-dimethylimidazolium 4-carboxylate.
We have found that this object is achieved by a process for the preparation of 1,3-dimethylimidazolium 4-carboxylate which involves reacting 1-methylimidazole with dimethyl carbonate.
From EP-A-291 074, it is known that dimethyl carbonate acts as a methylating agent during its reaction with an approximately stoichiometric amount of a tertiary amine. Thus, for example, the reaction of triethylamine with dimethyl carbonate gives the product triethylmethylammonium methyl carbonate in 89.9% yield (loc. cit., Example 1).
Synthesis, (1986) 382-3 and Liebigs Ann. Chem., (1987), 77-9 describe the synthesis of 1-methylimidazole in 91% yield by reacting imidazole with dimethyl carbonate in the presence of a catalyst. According to Liebigs Ann. Chem. (1987), page 77, 2nd column, 4th paragraph, the missing 9% yield can be attributed to unreacted imidazole. This publication also teaches that an attack by the imidazole or the 1-methylimidazole on the carbonyl group of the dimethyl carbonate does not take place.
Furthermore, from JP-A-10 17,553 (Chem. Abstracts 128: 167423p) and from JP-A-10 17,554 (Chem. Abstracts 128: 167424q), it is known that N-alkylimidazolines are methylated by reaction with dimethyl carbonate on the nitrogen atom in the 3-position. Thus, the reaction of 1-ethyl-2-methylimidazoline with (MeO)
2
CO gives the product 1-ethyl-2,3-dimethylimidazolinium methyl carbonate in 98% yield.
In the light of the documents cited above, it was to be expected that the reaction of 1-methylimidazole with dimethyl carbonate would give the product 1,3-dimethylimidazolium methyl carbonate in accordance with the equation below.
However, it has surprisingly been found that the reaction of 1-methylimidazole with dimethyl carbonate leads to 1,3-dimethylimidazolium 4-carboxylate of the formula I in high yields:
The novel process can be carried out as follows.
In general, 1-methylimidazole is initially introduced together with from 0.1 to 2 mole equivalents, preferably from 0.5 to 1.5 mole equivalents, particularly preferably from 0.9 to 1.1 mole equivalents, very particularly preferably 1 mole equivalent, of dimethyl carbonate, with or without a solvent, and the mixture is then heated to from 50 to 200° C., preferably from 100 to 180° C. with stirring.
In a preferred embodiment, the 1-methylimidazole is initially introduced, with or without a solvent, into the reaction vessel and is heated to from 50 to 200° C, preferably from 100 to 180° C., and to this is then added from 0.5 to 1.5 mole equivalents, preferably from 0.9 to 1.1 mole equivalents, particularly preferably one mole equivalent, of dimethyl carbonate.
Examples of suitable solvents are aliphatic or aromatic solvents, such as pentane, hexane, benzene, toluene, xylene, ethers, such as methyl tert-butyl ether, diethyl ether, tetrahydrofuran, dioxane, amides, such as dimethylformamide, dimethylacetamide, N-methylpyrrolidone, ureas, such as N,N′-dimethylethyleneurea, N,N′-dimethylpropyleneurea and N,N,N′,N′-tetra-n-butylurea, or additional dimethyl carbonate.
The reaction is particularly preferably carried out in the absence of a solvent.
The reaction times generally depend on the reaction temperature; the higher the chosen reaction temperature, the shorter is the reaction time. The reaction times are generally from 5 hours to 3 days, preferably from 12 to 24 hours.
The reaction is generally carried out at a pressure (measured in absolute terms) of from 0.05 to 5 MPa, preferably from 0.1 to 1 MPa. The reaction is particularly preferably carried out in a closed reaction vessel under autogenous pressure.
The reaction can be carried out either continuously or batchwise in common reaction vessels or reactors, such as stirred reactors, tubular reactors, battery of stirred containers.
The reaction product I is expediently purified by crystallization. Suitable solvents for this purpose are alcohols, such as methanol, ethanol, propanol, ethers, such as methyl tert-butyl ether, diethyl ether, tetrahydrofuran, dioxane, ketones, such as acetone, diethyl ketone, and esters, such as ethyl acetate.
REFERENCES:
patent: 5856513 (1999-01-01), Ue et al.
patent: 291 074 (1988-11-01), None
Tetrahedron Lett. 38, 3883-4 (1997).
Tetrahedron 29, (1973) 3135-6.
OZ 49266 = German 198 364 74.1.
Synthesis, 382-3 (1986).
Liebigs Ann. Chem. 1987 77-79.
JP Abstr. 128:167423p.
JP Abstr. 128:167424q.
Bomm Volker
Fischer Jakob
Fischer Martin
Mundinger Klaus
Siegel Wolfgang
BASF - Aktiengesellschaft
Keil & Weinkauf
Liu Hong
Shah Mukund J.
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