Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Patent
1997-03-14
1998-07-21
Higel, Floyd D.
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
5483255, 5483261, C07D23332, C07D23358
Patent
active
057837066
DESCRIPTION:
BRIEF SUMMARY
This application is a 371 of PCT/EP95/02806, filed Jul. 20, 1994.
The present invention relates to the preparation of 1,3-disubstituted 2-imidazolidinones from 1,3-dioxalan-2-one (ethylene carbonate) and primary amines.
1,3-Disubstituted 2-imidazolidinones, in particular 1,3-dimethyl-2-imidazolidinone, are interesting polar, aprotic solvents in particular for high molecular weight compounds such as polyamides, polyvinyl chloride, polyvinyl alcohol, polystyrene, polyurethane and phenol resins. Furthermore, 1,3-disubstituted 2-imidazolidinones are used in the textile industry as finishing agents.
Synthesis of 1,3-disubstituted imidazolidinones has been described many times. Catalytic hydrogenation of 1,3-dimethoxymethyl- or 1,3-dihydroxymethyl-2-imidazolidinone formed as intermediate and of other N,N'-dihydroxymethyl-substituted cyclic ureas (U.S. Pat. No. 2,422,400; U.S. Pat. No. 4,617,400) takes place with extensive residue formation. Alkylation of cyclic ureas (Synthesis (1982), 464; J. Med. Chem. 24, 1089, (1981)) requires besides the stoichiometric amount of a base toxicologically objectionable alkyl halides. Reactions of N,N'-disubstituted diamines with urea (EP 198 345), which must be carried out in a solvent, or with the toxicologically objectionable phosgene (EP 183 076) are likewise known. Also described are syntheses from carbon dioxide, primary amine and ethylene glycol (JP 5 9155-364-A) or dichloroethane, and the Leukart-Wallach reaction for synthesizing 1,3-dimethylimidazolidinone, which requires a heterogeneous hydrogenation catalyst (GB 1517820; DE 1545614; U.S. Pat. No. 2,422.400).
It is an object of the present invention to develop a synthetic route for 1,3-disubstituted 2-imidazolidinones which is simple and economic. It is intended in particular that the process be superior to known synthetic routes from the environmental viewpoint.
We have found that this object is achieved by a process as defined in the claims. Preferred embodiments are indicated in the dependent claims and in the following description.
It has been found, surprisingly, that ethylene carbonate can be reacted with primary amines to give the required cyclic urea directly without solvent or catalysts being necessary.
The invention therefore relates to a process for preparing 2-imidazolinones of the general formula (I) ##STR1## in which the radicals R, which can be identical or different, are a) straight-chain, branched or cyclic alkyl radicals with 1 to 12 carbon atoms, which can in turn be substituted by C.sub.6-10 -aryl, F, Cl, Br; substituted by C.sub.1-12 -alkyl; interrupted by one or more heteroatoms selected from O, S and N, heteroatoms selected from O, S, N, least one compound of the general formula (II) 1,3-dimethyl-2-imidazolidinone.
The reaction is generally carried out at from 150.degree. C. to 300.degree. C., preferably 200.degree. C. to 250.degree. C., particularly preferably under autogenous pressure. The autogenous pressure which is set up is usually from 50 to 150 bar, depending on the amine.
The amount of primary amine employed relative to ethylene carbonate is advantageously stoichiometric or more than stoichiometric, eg. 5.times.stoichiometric, preferably in the region of a 1.5 to 3.times.stoichiometric excess.
A reaction time of up to about 24 hours has frequently proven sufficient.
The yield of the process can generally be increased by using water. The amount of water employed can be up to 50% by weight, advantageously 30 to 45% by weight, based on ethylene carbonate employed.
The reaction mixture can be worked up by simple distillation of the crude product.
EXAMPLE 1
500 g of ethylene carbonate, 500 g of methylamine and 200 g of water were introduced at room temperature into an autoclave and heated at 250.degree. C. for 24 hours. The autogenous pressure of the reaction reached 120 bar.
The mixture was subsequently cooled, decompressed and distilled. 550 g of 1,3-dimethyl-2-imidazolidinone (R=CH.sub.3 in formula (I)) (85% of theory) were obtained at 60.degree. C. under 2 mbar.
EXAMPLE 2
The same m
REFERENCES:
patent: 2422400 (1947-06-01), Farlow
patent: 2892843 (1959-06-01), Levine
patent: 4617400 (1986-10-01), Ito et al.
Bogatsky et al., Synthesis, 1982, pp. 464-465.
Li et al., J. Med. Chem., vol. 24, 1981, pp. 1089-1092.
Mikheev et al., J. Org. Chem. USSR, 1983, pp. 436-439.
Dyer et al., J. Amer. Chem. Soc., vol. 79, 1957, pp. 672-675.
Henkelmann Jochem
Ruhl Thomas
BASF - Aktiengesellschaft
Higel Floyd D.
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