Claims
- 1. An optically active (meth)acrylamide monomer of the formula ##STR9## in which R.sup.1 represents hydrogen or methyl, and
- R.sup.2 represents one of the stereoisomers of the eight possible stereoisomeric forms of each of the optically active radicals of the formulae ##STR10##
- 2. A compound according to claim 1, in which
- R.sup.1 represents hydrogen or methyl, and
- R.sup.2 represents one stereoisomer of the eight possible stereoisomeric forms, in each case, of the optically active radical of the structural formula ##STR11##
- 3. A monomer according to claim 1 which is one stereoisomeric form of l-menthyl(meth)acrylamide.
- 4. A monomer according to claim 1 which is one stereoisomeric form of d-menthyl(meth)acrylamide.
- 5. A monomer according to claim 1 which is one stereoisomeric form of d-neomenthyl(meth)acrylamide.
- 6. An optically active and vinyl cross-linked polymer containing the repeating structural unit ##STR12## in which R.sup.1 represents hydrogen or methyl, and
- R.sup.2 represents one of the stereoisomers of the eight possible stereoisomeric forms of each of the optically active radicals of the formulae ##STR13##
- 7. An optically active and cross-linked polymer according to claim 6 with the following properties: ##EQU4## measured in toluene/ethyl acetate (ratio by volume 3:2), bulk volume[ml/g]: 1.52-2.5;
- particle size distribution: 1-500;
- nitrogen content [%] (without N in the crosslinker): 3.5-6.3,
- nitrogen content [%] (with N in the crosslinker): 6.3-13.
- 8. A copolymer consisting essentially of monomer units according to claim 6 and 0.5 to 50 mol % of monomer units of a cross-linking agent.
- 9. A copolymer according to claim 8, containing 1 to 20 mol % of monomer units of the cross-linking agent.
- 10. A copolymer according to claim 8, containing 5 to 15 mol % of monomer units of the cross-linking agent.
- 11. A copolymer according to claim 8, wherein the cross-linking agent is a monomer containing two vinyl groups.
Priority Claims (1)
| Number |
Date |
Country |
Kind |
| 3532356 |
Sep 1985 |
DEX |
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Parent Case Info
This is a division of application Ser. No. 925,340, filed Oct. 31, 1986, now abandoned, which is a continuation-in-part of application Ser. No. 904,734, filed Sept. 5, 1986, now abandoned.
The invention relates to optically active (meth)acrylamides, the optically active polymers prepared therefrom, processes for the preparation of the optically active monomers and polymers, and the use of the polymers as adsorbents, in the particular as the stationary phase for chromatographic racemate resolution.
The separation of racemic mixtures into the antipodes represents a considerable problem in preparative chemistry. Chromatographic separation methods using optically active adsorbents as stationary phase are becoming increasingly important for this purpose. However, the results hitherto have been less than satisfactory. Thus, the separating effect of the optically active adsorbents which are disclosed in DE-OS (German Published Specification) No. 2,500,523 is, for some racemates of certain classes of substances, so small that there are clear limits to the industrial applicability of a racemate resolution of this type.
It has now been found that an especially good separation efficiency can be obtained by use of certain optically active (meth)acrylamide polymers.
Thus the invention relates to optically active (meth)acrylamide monomers of the general formula 1 ##STR3## in which R.sup.1 represents hydrogen or methyl, and
Preferred compounds of the formula 1 are those in which
L-Menthyl(meth)acrylamide, d-menthyl(meth)acrylamide and d-neomenthyl(meth)acrylamide are particularly preferred.
The monomer according to the invention are obtained by reaction of optically active amines of the formula (2)
Groups which can be eliminated and which may be mentioned are: halogen, in particular chlorine or bromine, or a group of the formula OR.sup.3, in which R.sup.3 represents a C.sub.1 -C.sub.4 -alkyl group, or a ##STR7## group. Furthermore, it is also possible to use unsymmetrical acid anhydrides.
The acrylic acid derivatives of the formula 3 which are used as starting materials are known [Beilsteins Handbuch der organischen Chemie (Beilstein's Handbook of Organic Chemistry), Volume 2, 3rd supplement, page 1293; Volume 2, original edition, page 400].
The optically active amines of the formula 2 which are used as starting materials are known or can be prepared by known methods (E. Beckmann, Liebigs Ann. Chem. 250, 322 ff (1889), H. C. Brown, P. C. Garg, J. Am. Chem. Soc. 83, 2952 (1961), F. Tutin, F. S. Kipping, J. Chem. Soc. London 85, 65-78 (1904), J. Read, Chem. Rev. 7, 1 (2930), H. Feltkamp, F. Koch und Tran Nhut Thanh, Liebigs Ann. Chem., 707, 78 (1967).
Suitable acid addition compounds of the amines used according to the invention are salts of these amines with inorganic or organic acids. Mineral acids such as, for example, hydrochloric acid, hydrobromic acid, sulphuric acid or phosphoric acid, methanesulphonic, ethanesulphonic, benzenesulphonic or toluenesulphonic acid, are preferred.
All inert organic solvents are suitable as solvents. Hydrocarbons such as, for example, benzene, toluene, xylene or petroleum fractions, or halogenated hydrocarbons such as, for example, dichloromethane, trichloromethane or tetrachloromethane, dichloroethane or trichloroethylene, are preferred.
The customary inorganic and organic bases are suitable as bases. Alkali metal or alkaline earth metal hydroxides such as, for example, sodium, potassium, lithium, calcium or barium hydroxide, alkali metal or alkaline earth metal carbonates such as, for example, sodium or potassium carbonate, alkali metal alcoholates such as, for example, sodium ethanolate, potassium ethanolate, sodium methanolate or potassium methanolate, or amines such as, for example, triethylamine, pyridine, morpholine or piperidine, are preferred.
The reaction temperatures can be varied within a relatively wide range. In general they are in the range from -20.degree. C. to +100.degree. C., preferably from -10.degree. C. to +60 .degree. C.
The reaction can be carried out under atmospheric, elevated or reduced pressure. In general it is carried out under atmospheric pressure.
The compounds of the formulae 2 and 3 are preferably used in equimolar ratios.
The invention also relates to optically active crosslinked polymers which contain the repeating structural unit ##STR8##
These polymers have the following properties: ##EQU1## measured in toluene/ethyl acetate (ratio by volume 3:2) bulk volume [ml/g]: 1.5-2.5; preferably 1.6-2; particularly preferably 1.6-1.8, particle size distribution [.mu.m]: 1-500; preferably 1-200; particularly preferably 1-100, nitrogen content [%] (without N in the crosslinker): 3.5-6.3, preferably 4.5-6.2; particularly preferably 5.5-6; nitrogen content [%] (with N in the crosslinker): 6.3-13; preferably 6.5-10; particularly preferably 6.5-7.5,
These polymers according to the invention are prepared by polymerization, in a manner known per se, of the monomer of the formula 1 with 0.5 to 50 mol-%, preferably with 1 to 20 mol-%, in particular with 5 to 15 mol-% (relative to 1 mol of monomer) of a suitable crosslinker.
The invention preferably relates to a process in which the polymerization is carried out as suspension polymerization using an inert organic phase and an aqueous solution of a protective colloid.
The invention particularly relates to a process in which the suspension polymerization is carried out using toluene or chloroform as inert organic phase and an aqueous solution of a protective colloid consisting of a copolymer of methacrylic acid with methyl methacrylate as aqueous phase.
The suspension polymerization of the monomers according to the invention, of the formula I, can also be carried out, in a manner known per se, in the presence of an additional radical-forming agent.
Suitable crosslinking agents are compounds which contain at least two polymerizable vinyl groups. Preferred crosslinking agents are alkanediol diacrylates having about 8 to 12, preferably having 8 to 10, carbon atoms, such as, for example, 1,4-butanediol diacrylate, 1,3-propanediol diacrylate or 1,2-ethylene glycol diacrylate, or alkanediol dimethacrylates having about 10 to 14, preferably having 10 to 12, carbon atoms, such as, for example, 1,4-butanediol dimethacrylate, 1,3-propanediol dimethacrylate or 1,2-ethylene glycol dimethacrylate, aromatic divinyl compounds such as, for example, divinylbenzene, divinylchlorobenzene or divinyltoluene, vinyl esters of alkanedicarboxylic acids having about 8 to 14, preferably having 8 to 10, carbon atoms, such as, for example, divinyl adipate, divinyl benzenedicarboxylate, divinyl terephthalate, N,N'-alkylenediarylamides having about 8 to 12, preferably having 8 to 10, carbon atoms, such as, for example, N,N'-methylenediacrylamide, N,N'-ethylenediacrylamide, N,N'-methylenedimethacrylamide or N,N'-ethylenedimethacrylamide.
Suitable radical-forming agents are the customary radical-forming agents. Peroxides such as, for example, dibenzoyl peroxide, dilauroyl peroxide or di-orthotolyl peroxide, or azo compounds such as, for example, azobisisobutyronitrile (AIBN), are preferred.
The reaction components are dissolved in an organic solvent, preferably an aromatic hydrocarbon, such as benzene or toluene, or a halogenated hydrocarbon, such as dichloromethane, trichloromethane, tetrachloromethane or 1,2-dichloroethane.
It has proved to be advantageous for this to use as little solvent as possible. The lowermost limit of this is determined by the solubility of the monomers. It is particularly advantageous to use about 1 part by weight of solvent for each part by weight of monomer, or sufficient solvent just to dissolve the monomers. The organic phase is thoroughly dispersed in an aqueous solution of a protective colloid, preferably in an aqueous solution of a copolymer of methacrylic acid and methyl methacrylate, using an efficient stirrer. About 1 to 20, preferably about 2 to 10, parts by weight of the aqueous phase are used for each part by weight of organic phase. The stirred mixture is heated under an inert gas atmosphere, preferably under nitrogen, at temperatures between 30.degree. C. and 100.degree. C., preferably between 40.degree. C. and 80.degree. C. The polymerization time is between 4 and 12, preferably between 4 and 8, hours. The copolymer obtained in this manner is removed from the reaction mixture by filtration, purified by thoroughly washing with water and with organic solvents such as methanol, ethanol, benzene, toluene, dichloromethane, trichloromethane or acetone, and is then dried.
The polymer which is particularly preferably prepared by the process described above is that of L-d-menthyl(meth)acrylamide or d-neomenthyl(meth)acrylamide.
The invention also relates to the use of the polymers according to the invention for the chromatographic separation of racemic mixtures into the optical antipodes.
In particular, the invention relates to the use of the polymers according to the invention for the chromatographic resolution of active compound racemates into the optical antipodes, such as, for example, derivatized aminoacids, .beta.-lactam compounds, pyrethroids, pyrethroid acids, monocyclic or bicyclic terpene derivatives, nitro- or cyanodihydropyridines, dihydropyridinecarboxylic acids, esters or amides, dihydropyridinelactones or sulphonyldihydropyridines.
Surprisingly, the polymers according to the invention have a better separation efficiency than those known from the state of the art. Thus, the optical yield on resolution of the racemate of methyl 1,4-dihydro-2,6-dimethyl- 5-nitro-4-(2-trifluoromethylphenyl)-pyridinecarboxylate on the adsorbent according to the invention is 71% compared with 50% on the adsorbent which is disclosed in DE-OS (German Published Specification) No. 2,500,523 and consists of a copolymer of the (S)-1-phenylethylamide of methacrylic acid and 1,4-butanediol dimethylacrylate. Furthermore, the polymer according to the invention exhibits a good separation efficiency even on separation of relatively large amounts of racemic mixtures, which is a great advantage for industrial use.
The preparative separation of racemic mixtures into their optical antipodes using the polymers according to the invention is advantageously carried out by column chromatography. It is particularly advantageous in this to carry out the chromatographic separation with polymers which have been graded according to particle size, in order to obtain optimum separation efficiencies. Graded polymers of this type can be prepared in a manner known per se, for example by screening or air-sifting of the polymers according to the invention.
The methods of carrying out separation by column chromatography are familiar to the expert. Normally, the polymer is suspended in the mobile phase, and the suspension is introduced into a glass column. After the mobile phase has run out, the racemate which is to be resolved, dissolved in the smallest possible amount of mobile phase, is applied to the column. Then elution with the mobile phase is carried out, the eluate being collected in fractions as usual.
The mobile phases which are used are the customary organic solvents or mixtures of solvents which induce the polymer which is used as adsorbent to swell and which are able to dissolve the racemate which is to be resolved. Examples which may be mentioned in this context are: hydrocarbons such as benzene, toluene or xylene, ethers such as diethyl ether, dioxane or tetrahydrofuran, halogenated hydrocarbons such as dichloromethane or trichloromethane, acetone, acetonitrile or ethyl acetate, as well as mixtures of the said solvents.
Mixtures of toluene and ethyl acetate have proved to be especially suitable.
The composition of the mobile phase can be selected and optimized in a customary manner depending on the nature and property of the racemate which is to be resolved.
The separation efficiency of the polymer according to the invention is illustrated by means of a few racemates, using the capacity ratio k'.sub.1 k'.sub.2 and the enantioselectivity .alpha., k'.sub.1, k'.sub.2 and .alpha. being defined as follows: ##EQU2##
US Referenced Citations (1)
| Number |
Name |
Date |
Kind |
| 4138542 |
Sieget et al. |
Feb 1979 |
|
Foreign Referenced Citations (6)
| Number |
Date |
Country |
| 0121618 |
Oct 1984 |
EPX |
| 0218089 |
Apr 1987 |
EPX |
| 2500523 |
Jul 1976 |
DEX |
| 0013416 |
Dec 1979 |
DEX |
| 3532356 |
Mar 1987 |
DEX |
| 2354351 |
Jan 1978 |
FRX |
Non-Patent Literature Citations (5)
| Entry |
| Makromol. Chem. Rapid Commun 1, 85-89 (1980) Blaschke et al. |
| Chemical Society Journal (London/pp. 2168-2170, 2222 Reed et al (1926). |
| John Read et al, "Researches in the Menthone Series . . . ", J. Chem. Soc. London (1927), pp. 2168-2170. |
| Feltkamp et al, "Synthese und Trennung der 8 Menthyl- und Carvomenthylamine", Liebigs Ann. Chem. 707, p. 78. |
| Streitwieser et al, "Organische Chemie", Verlag Chemie (1980), p. 140. |
Divisions (1)
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Number |
Date |
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| Parent |
925340 |
Oct 1986 |
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Continuation in Parts (1)
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Number |
Date |
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| Parent |
904734 |
Sep 1986 |
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Patent Grant
4931525
