US20060014955A1

US20060014955A1 - Optically enhanced chiral ionic liquids

Info

Publication number: US20060014955A1
Application number: US11/177,093
Authority: US
Inventors: Daniel Armstrong; Jie Ding
Original assignee: Advanced Separation Technologies Inc
Current assignee: Sigma Aldrich Co LLC
Priority date: 2004-07-09
Filing date: 2005-07-08
Publication date: 2006-01-19
Also published as: CA2573078A1; CN101035523A; AU2005271958A1; US7776582B2; MX2007000253A; JP2008505918A; EP1765781A2; US20090145197A1; WO2006017148A3; WO2006017148A2

Abstract

The invention relates to the use of optically enhanced chiral ionic liquids, particularly for gas chromatography and as a reaction solvent. Specific optically enhanced chiral cationic liquids are described as is a class of optically enhanced chiral anionic liquids.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of the filing date of U.S. Provisional Patent Application No. 60/586,782 filed Jul. 9, 2004, the disclosure of which is hereby incorporated herein by reference.

BACKGROUND OF THE INVENTION

Nonchiral ionic liquids have been used as solvents in the past. Chiral liquids that are racemic have been used as solvents as well. See Yasuhiro Ishida et al., “Design and synthesis of a novel imidazolium-based ionic liquid with planar chirality,” Chem. Commun. 2240-41 (2002) (a copyright of the Royal Society of Chemistry). Solvents of enantiomerically enhanced chiral cations have also been described. See Wasserscheid et al., “Synthesis and properties of ionic liquids derived from the ‘chiral pool’,” Chem. Commun. 200-01 (2002) and Weiliang Bao et al., “Synthesis of Chiral Ionic Liquids from Natural Amino Acids,” 68 J. Org. Chem. 591 (2003). These were not described as vehicles for conducting subsequent reactions.
Earle et al. disclosed reactions of dienes and dienophiles in various solvents including [bmim] [lactate], an ionic liquid with a chiral anion of unreported configuration or purity. The result was not asymmetric. See Martyn J. Earle et al., “Diels-Alder reactions in ionic liquids,” Green Chem. 23-25 (1999). Chiral nonionic materials have also been used as the stationary phases in gas chromatography. (See U.S. Pat. Nos. 4,948,395 and 5,064,944.)

SUMMARY OF THE INVENTION

The present invention relates to optically enhanced chiral ionic liquids (“OCIL”). These are salts which are liquids having a melting point of 100° C. or less. Preferably, they are liquid at room temperature (18° C. to about 25° C.) or less.
OCILs in accordance with the present invention are liquid materials made from chiral compounds and/or their salt mixtures and associations thereof. “Chiral” as used herein means that the compound has at least one stereogenic center or axis (also referred to as a “chiral center” or “asymmetric center”). “Ionic” as used in connection with OCILs in accordance with the present invention includes cations, anions or salts thereof. A chiral anion is an anion which contains a stereogenic center or axis. A chiral cation is a cation which contains a stereogenic center or axis. OCILs may also be salts, mixtures or associations of both chiral cations and chiral anions. Thus a chiral anion may be associated with a nonchiral cation, thus forming a “chiral anion containing OCIL,” also referred to herein as a “chiral anion” or an “anionic OCIL,” or may be associated with a chiral cation. Similarly, a chiral cation may be associated with a nonchiral anion thus forming a “chiral cation containing OCIL,” also referred to herein as a “chiral cation” or a “cationic OCIL” or it may be associated with a chiral anion.
Many of the compounds discussed herein are enantiomers, pairs of mirror image compounds with opposite optical configurations, (each referred to as an enantiomer or an optical isomer as appropriate). These can be present in the form of either a racemic (50:50) mixture or an optically enhanced mixtures in which one of the enantiomers is present in an amount which is greater than the other. “Optically enhanced,” even when described in the context of an optically enhanced mixture, also is meant to include an optically pure material which is substantially or completely only one of the two enantiomers. The OCILs of the invention are not limited to enantiomers, but may include diastereoisomers, compounds that have more than one stereogenic center. A compound of this type with, for example, 2 stereogenic centers can be thought of for the invention as producing two distinct sets of enantiomers. Of course, while each enantiomer will be present as an equal mixture, one pair of enantiomers may be present in a greater percentage than the other. An OCIL in the case of diastereoisomers is a compound which meets the other criteria set forth herein wherein at least one of the enantiomers is present in an enhanced amount relative to its corresponding enantiomer. The other enantiomeric pair may still be racemic relative to each other, or one of optical isomers of that pair of enantiomers may also be optically enhanced. Thus it is still proper, in the context of the invention to refer to racemic mixtures and enantiomers, even though they may be diastereoisomers relative to other possible optical isomers.
One aspect of the present invention is the discovery of a novel class of chiral cationic containing OCIL molecules (often used synonymously with the term “compound” herein or as the context indicates) and in particular, those individually identified herein. Another aspect of the invention are chiral cationic containing OCILs in which at least one enantiomer is enhanced by at least about 2% relative to the other. Another aspect of the invention are chiral cationic containing OCILs in which at least one enantiomer is enhanced by at least about 10% relative to the other. Another aspect of the invention are chiral cationic containing OCILs in which at least one enantiomer is enhanced by at least about 20% relative to the other. In another aspect, the invention relates to chiral cationic containing OCIL molecules which are other than N-alkyl-N-methylephedrinium salts, and/or those shown in Table A.
Another aspect of the present invention is the discovery of a class of anionic containing OCILs. One aspect of the invention are chiral anionic OCILs in which at least one enantiomer is enhanced by at least about 2% relative to the other. Another aspect of the invention are chiral anionic containing OCILs in which at least one enantiomer is enhanced by at least about 10% relative to the other. Another aspect of the invention are chiral anionic containing OCILs in which at least one enantiomer is enhanced by at least about 20% relative to the other. In another aspect of the invention, there are provided anionic containing OCILs that are not lactates.
In yet another aspect of the present invention there is provided a class of OCILs which are salts where both anions and cations are chiral, and at least one, and preferably both, are optically enhanced. In another embodiment of this aspect of the present invention, both the cationic and anionic portions of the OCIL are chiral, but have an opposite optical rotation. Thus, for example, the cation may be (R) and the anion (S). Indeed, in this situation, there could be each of a cation with an (R) configuration, a cation with an (S) configuration, an anion with an (R) configuration and an anion with an (S) configuration, in various proportions. Thus the combinations of chiral cation and chiral anion include (R)(S), (S)(R), (R)(R), (S)(S), and preferably these are substantially pure.
In yet another aspect of the present invention there is provided a solvent that may be used for dissolving, suspending, gelling, emulsifying, dispersing and forming colloids, comprising chiral anionic, chiral cationic or mixed anionic and cationic containing OCILs. These may include those of Table A.
Another aspect of the present invention is a method of conducting a chemical reaction in the presence of at least one chiral cationic and/or chiral anionic containing OCIL. These may include those of Table A. The OCIL can be present as a part of a solvent system or as the reaction medium or carrier for one or more of the reactants or even as a reactant. Also considered part of the invention are molecules, whether chiral or achiral, racemic or not, pharmaceutically or chemically active/reactive or inert, finished product or intermediate resulting from a chemical reaction conducted in the presence of any OCIL. Preferred are non-racemic compounds synthesized asymmetrically using an OCIL in accordance with the invention. Also preferred are any reactions that are enantiomerically (or optical isomerically) selective. Also preferred are reactions using or in the presence of OCILs which involve the use of a charged species (other than the OCIL) as a reactant, reagent, intermediate or final product.
Reactions include, without limitation, condensation, hydrogenation, nucleophilic and electrophilic substitutions, deracemization, asymmetric synthesis, esterification, ether formation, halogenation, polymerization reactions, chain propagation, cross-linking, salt formation, precipitation or crystallization and the like. Deracemization and asymmetric synthesis reactions are particularly preferred. Also preferred are any reaction of the type noted immediately above that is enantiomerically (or optical isomerically) selective. Also preferred are those reactions noted immediately above using OCILs which involve the use of a charged species (other than the OCIL) as a reactant, reagent, intermediate or final product. In accordance with another aspect of the invention, any of the foregoing reactions are conducted in the presence of an OCIL which is enhanced such that it is substantially optically pure (at least 90% of one enantiomer relative to the other enantiomer). Preferably these reactions using substantially pure OCILs include asymmetric synthesis, deracimization, reactions using charged species and enantioselective processes.
A particularly preferred aspect of the present invention is an asymmetric synthesis of a compound comprising the steps of conducting a chemical reaction on at least one reactant which is in the presence of an OCIL to produce a reaction product. The reaction product is recovered and it is optically active, i.e., it has a stereogenic center or axis. One enantiomer of the reaction product will be present in an amount that is greater than the other enantiomer, usually at least about 2% difference or more (52:48%). Preferably the OCIL is the solvent. More preferably, at least a 10% difference, even more preferably at least a 20% difference, even more preferably a substantially pure OCIL is found between the content of enantiomers.
Another particularly preferred aspect of the present invention is a deracemizing reaction wherein a reactant which is in the presence of an OCIL is reacted to form a reaction product. The reactant is racemic and the reaction product, while optically active, is not racemic. Again, preferably the amount of one enantiomer is at least 2% greater than that of the other (52:48%), more preferably one reaction product is enhanced so at least about 10% more of one enantiomer is present compared to the other, even more preferably the difference is at least about 20%, and most preferred is substantially pure. Preferably the OCIL is a solvent. The asymmetric products of these reactions run in the presence of an OCIL are also claimed. These reaction products may also be separated to produce a substantially optically pure reaction product.
Another aspect of the present invention relates to the use of cationic and/or anionic OCILs as the stationary phase or support in columns prepared for chromatography including liquid chromatography, gas chromatography (“GC”) and in particular capillary GC. In particular there is provided a column for use in chromatography comprising: a column and a stationary phase which is an OCIL associated therewith. Any OCIL may be used as a stationary phase. In one embodiment, the column is a capillary and the OCIL stationary phase is coated on an inner surface of said capillary. The column in accordance with the invention may also be a packed column wherein the stationary phase is absorbed, adsorbed or coated on a solid support which is packed into the column.
The invention also includes methods of separating compounds comprising the steps of: mixing, dissolving, dispersing or suspending optical isomers in a mobile phase which can be a gas or a liquid depending upon the type of chromatography, introducing the compounds to be separated into a column that includes at least one OCIL, either coated on the inside thereof or as part of a packing as a stationary phase, and advancing the mobile phase and at least one of the compounds to be separated through the column so as to resolve at least one of compounds to be separated. In a particularly preferred aspect of the invention, the compounds to be separated are optical isomers.

DETAILED DESCRIPTION

By “optically enhanced” it is understood that the chiral compounds of the invention are not present in a racemic mixture (both enantiomers present in approximately the same percentage). Instead, in accordance with the present invention, at least one of the enantiomers is present in a greater percentage. As noted previously, this applies to diastereomers as well wherein at least one of the enantiomers of one of the pairs of optical isomers which are identical but for their configuration is present in an amount that is greater than the other. More preferably, the one enantiomer is present in an amount of at least about 2.0% greater than the other enantiomer by mole percent or weight percent, as is appropriate. More preferably, one of the optical isomers will be present in an amount of at least about 10% greater than the other and even more preferably an amount of at least about 20% than the other optical isomer of a pair of enantiomers. Even more preferably, such compounds are “substantially optically pure,” wherein about 90% or more of the compound in question will be a single enantiomer. This is of course relative to the other enantiomer. Diastereomers with two stereogenic centers, for example, could be substantially optically pure in the context of the invention if it had 90% of one optical isomer, 10% of its enantiomer, yet 53 percent of the total composition was a racemic mixture of the other set of enantiomers. Most preferably, an OCIL will have at least one enantiomer be present in 95% or greater relative to the other.
In the case of a mixed solvent or stationary phase of two or more chiral ionic liquids, it is not necessary that all of the liquids be optically enhanced OCILs. One or more may be racemic as long as at least one is optically enhanced.
OCILs have been found to have many uses. It has been found that they are useful as solvents, dispersants, gelling agents, emulsifying agents, colloid forming agents, and suspending agents. Indeed, because of their ability to interact on almost any level with almost any other molecule, OCILs may often be substituted, in whole or in part, for traditional organic solvents and water. OCILs can interact not only ionically, but also through, for example, dipole interaction, hydrogen bonding, pi-pi (n-n) interaction, dispersion interactions and even steric forces. This makes them useful in chemical reactions, whether used as a reactant, a solvent, or merely present during a reaction. In addition, the ability to use a material that is at least predominantly one optical isomer or another provides another dimension to research and manufacturing. It allows for potentially different interactions, using a solvent of the same chemical. The enhanced level of one optical isomer, or preferably, their substantially optically pure nature, will allow them to interact in previously unimagined ways. This is particularly true for mixtures of chiral cations and chiral anions which my have the same optical rotation of may have opposite rotations.
These OCILs are considered “green” in that they are recyclable alternatives to volatile organic solvents. They are air and moisture stable, have excellent solubilizing properties and virtually no vapor pressure. They are nonaqueous, although they can be mixed with water, and therefore can be used in a variety of situations where water is inappropriate.
OCILs in accordance with one aspect of the present invention include optically enhanced chiral cations such as, without limitation, (−)-N-Benzyl-N-methylephedrinium.NTf₂Isoleucine-based ILs, as either an ester or an alcohol, (−)Cotinine.TfO, D(+)-Carnitinenitrile.NTf₂, 1-((R)-1,2-propanediol)-3-methylimidazolium chloride, (−)-Scopolamine N-butyl.NTf₂and (+)-chloromethyl methyl ether imidazolium IL. Their structures are as follows:
Some of these chiral cationic containing OCILs can be produced by the following general reactions:
The above are merely examples of chiral cationic containing OCILs in accordance with one aspect of the present invention. Each are individually considered to be part of the invention. Other cationic OCILs can be produced by methods described in the art. See Wassefscheid and Bao, supra. To qualify as a chiral cationic containing OCIL, a molecule should meet at least some of the following criteria. It should have at least one stereogenic center or axis and be capable of being synthesized as an ionic material which has a melting point of 100° C. or less, and most preferably be a liquid at room temperature (18° C.-25° C.) or below. It should contain a greater amount of one optical isomer relative to its enantiomer optical isomers of the same molecule in the system or mixture. Preferably, it is substantially optically pure. Preferably, at least 95% w/w of at least one enantiomer of the molecule is in the form of one optical isomer. To be a chiral cationic containing OCIL, it must also have a positive charge overall.

The class of novel chiral cation containing OCILs excludes these molecules as shown in Table A.

TABLE A



1

2

3

4

5

6

7

8

9

10

11

12

The molecules shown in Table A having an enhanced optical purity and in particular a purity whereby one enantiomer is present in an amount of at least about 10% greater than the other, more preferably 20% greater than the other, and even more preferably substantially optically pure are contemplated as part of the invention. Moreover, the use of the molecules shown in Table A as a stationary phase in chromatography, as a solvent or other use in chemical reactions described herein are also considered part of the invention.
OCILs in accordance with the present invention also include those that are anionic. These have the same overall properties as the chiral cationic containing OCILs except that they have the opposite charge. These chiral anionic containing OCILs include, but are not limited to, those with the following structures:

This material can be made by the following general reaction:
Other non-limiting examples of chiral anions for OCILs (illustrated with a sodium cation and thus more correctly are —O⁻ Na⁺):
A general reaction which can be used to produce anionic OCILs is as follows:
An anion exchange reaction can take place on the OH⁻ form strong anion exchange resin between an achiral or chiral IL containing an exchangeable anion (such as Br⁻, I⁻) and the resin. And then the hydroxide IL can further react with chiral compounds by means of carboxylic acid group. This finally results in anionic OCILs.
Salts created from either chiral cation containing OCILs and/or chiral anion containing OCILs are also included. These include an OCIL and a counter ion. Counter ions include, without limitation, PF₆—, [(CF₃SO₂)₂N—], (CF₃)SO₂ ⁻, Cl—, BMIM (butyl methyl imidazolium). Mixtures of these can also be created where the chiral anion containing OCIL and chiral cation containing OCIL are associated, as salts acting as counter ions for each other or disassociated. Such salts can be created from, for example, any of the anionic OCILs and cationic OCILs identified herein.
Another preferred aspect of the present invention involves conducting a chemical reaction in the presence of an OCIL, more preferably using an OCIL as a reaction medium, reaction solvent or cosolvent to form a reaction product. It is preferred that such OCILs be substantially optically pure. These reactions involve contacting or mixing one or more OCILs in accordance with the present invention with at least one reactant and causing a reaction to take place wherein some change occurs to the reactant (the “reaction product”). This change may be a change in physical state such as precipitating or melting, or maybe a change in a reactant's structure such as ionization, creation of a free radical and the like. The reaction may also include chemical reorganizations and/or oxidation/reduction reactions such as transfer of an aldehyde to ketone or alcohol to acid. Movement of an unsaturated bond, a change is a resonance, etc are also contemplated. Chemical reaction can also include: hydration, condensation, hydrogenation, nucleophilic and electrophilic substitutions, cyclization, esterification, ether formation, halogenation, polymerization reactions, chain propagation, cross-linking, salt formation, crystallization, nucleophilic or electrophilic addition or substitution, saturation or unsaturation. These are just some of the reactions which are possible. While the OCILs may participate in or facilitate these reactions, they generally will not actually be a participant in that they will generally not be part of the resulting chemical. Of course, it is not unusual for solvents to be contained within various materials such as crystalline materials in the form of solvates and that is not excluded.
Reactions that can be run using OCILs in accordance with the present invention include, without limitation, the following:
Oxidation

- 1. Oxidation of sulfides, selenides and amines to the corresponding oxides by NaIO₄. plus rearrangement of the corresponding allylic oxides to allylic alcohols.
- 2. Oxidation of alkenes to cis-1,2-diols by KMnO₄, OSO₄, and cat. OSO₄plus reoxidant.
- 3. Oxidation of alkenes to trans-1,2-diols by KHSO₅.KHSO₄.K₂SO₄plus water.
- 4. Oxidation of 2-naphthols to binaphthols by CuCl₂.4H₂O and FeCl₃.6H₂O and oxidation of 2-naphthylamines to binaphthyl diamines by CuCl₂.4H₂O.
- 5. Olefin epoxidation by peracids; H₂O₂plus urea, nitriles, tungstate, molybdate and vanadyl reagents; NaOCl plus Cr— or Mn(salen) complexes; NaIO₄plus Mn(III) or cat. RuCl₃; KMnO₄plus CuSO₄; methyltrioxorhenium and KHSO₅.KHSO₄.K₂SO₄.
- 6. Kinetic resolution of 2° alcohols [1-phenylethyl alcohol and 2-butanol] by oxidation with KMnO₄, tetra-N-propylammonium perruthenate and other oxidants.

Reductions

- 1. Reduction of ketones [PhCOMe and ethyl acetoacetate as model systems] to alcohols by NaBH₄, NaHB(OMe)₃, NaHB(OAc)₃and NaH₃BCN.
- 2. Reductive amination of ketones [PhCOMe and cyclohexyl methyl ketone as model systems] by various 10 and 20 amines using NaH₃BCN.

Pericyclic Reactions

- 1. Diels-Alder, hetero Diels-Alder and inverse electron-demand Diels-Alder reactions, particularly reactions that are reversible like those of furan. not run in lactate.
- 2. Cope and oxy-Cope rearrangements.
- 3. Claisen rearrangement.

Pd-Catalyzed Processes

- 1. Alkylation of allylic acetates by amines, stabilized carbanions and other nucleophiles.
- 2. Inter- and intramolecular Heck reactions using aryl halides/triflates, cycloalkenes and Pd(0).
- 3. Reaction of ArI(OTf) with R¹CH═CR²CHR³OH to give ArCHR¹CHR²COR³.
- 3. Suzuki reaction of hindered aryl halides/triflates and arylboronic acids to form atropisomers.
- 4. Pd(II)-catalyzed cyclization of 2-allylic phenols to 2,3-dihydrobenzofurans.
- 5. Pd(0)-catalyzed annulation of 1,2-, 1,3-, and 1,4-dienes by 2-haloanilines and -phenols.
- 6. Hydroesterification of styrenes to 2-arylpropionic acids and esters.

Other Transition Metal-Catalyzed Processes

- 1. Hydroformulation of internal olefins [cis-3-hexene, cyclopentene and cyclohexene].
- 2. Hydrogenation of RR′C═CH₂, H₂C═C(NHAc) CO₂H(R), H₂C═CArCO₂H(R) and Baylis-Hillman adducts.
- 3. Pauson-Khand reaction.
- 4. Conversion of RCH═CH₂and N₂CHCO₂R′ to cyclopropane esters.
- 5. Inter- and intramolecular hydroamination and hydroalkoxylation of alkenes by PtCl₂or Zn(OTF)₂.

Condensation Reactions

- 1. Michael reactions [cyclohexenone and MeCOCH₂COMe or EtO₂CCH₂CO₂Et].
- 2. Aldol [MeCHO] reaction.
- 3. Claisen condensation [ethyl propionate and ethyl phenylacetate].
- 4. Henry reaction of aldehydes [MeCHO and PhCHO] with nitroalkanes [MeNO₂].
- 5. Baylis-Hillman reaction [PhCHO and acrylates, acrylonitrile and methyl vinyl ketone using DABCO and BU₃P].
- 6. Cyanohydrin and silyl cyanohydrin formation from aldehydes [PhCHO].
- 7. Strecker synthesis of RCH(NH₂)CN from RCHO, NH₃and HCN.
- 8. Passerini synthesis of R¹CH(O₂CR²)CONHR³from R¹CHO, R²CO₂H and R³NC.
- 9. Ugi synthesis of R¹CH(NHR⁴COR²)CONHR³from R¹CHO, R²CO₂H and R³NC and R⁴NH₂.
- 10. Sc(OTf)₃-catalyzed condensation of ArCHO, PhNH₂and P(OEt)₃to industrially important ArCH(NHPh) PO(OEt) 2.

Alkylation Reactions

- 1. Alkylation of enamines [cyclohexanone pyrrolidine enamine and MeI].
- 2. Alkylation of unsymmetrical dicarbonyl compounds [ethyl acetoacetate, PhCOCH₂CO₂Et, PhCOCH₂COCH₃].
- 3. Friedel-Crafts arylation by 20 alkyl halides and triflates in non-alcohol containing CILs.

Other Organic Reactions

- 1. SN²reactions of 20 alkyl halides [PhCHBrMe model system] with various nucleophiles [NaOAc, NaN₃, NaOMe, NaSPh, NaOPh and Na(acac)] for the kinetic resolution of organic halides and synthesis of chiral products.
- 2. SN²ring opening of symmetrical epoxides [cis-2-butene oxide, cyclopentene oxide] by various nucleophiles.
- 3. Kinetic resolution of 20 alkyl esters [20 butyl and phenethyl acetates and benzoates] by hydrolysis and transesterification [MeOH and EtOH].

Particularly preferred are those reactions discussed above that are enantiomerically selective (applicable to diastereomers as noted previously) those that involve a changed reactant, reagent, intermediate or product, other than the OCIL. Also preferred are those reactions run in an OCIL that is substantially optically pure (at least 90 of one enantiomer relative to the other) as well as those run using chiral cationic containing OCILs and chiral anionic containing OCILs that are not lactates. Combinations of these are also preferred, such as, by way of a non-limiting example, those enantiomerically selective reactions run in a chiral anionic containing OCIL that is substantially optically pure. Many of these reactions, run in an OCIL, are particularly preferred as they permit the asymmetric synthesis of one enantiomer over another. This is a particularly preferred aspect of the invention.
A particularly preferred type of reaction in accordance with the present invention is deracemization. A deracemization reaction allows for the transformation of a racemic mixture of a chiral carbon-containing compound to a mixture in which one optical isomer predominates. Preferably, the one resulting optical isomer will be present in an amount greater than any other optical isomer of the same compound present. In a racemic mixture of enantiomers from a single chiral center, following a reaction in the presence of an OCIL, preferably one enantiomer will be provided in an amount greater than 50% with the balance being the other. In a particularly preferred aspect of the present invention, the deracemization reaction provides at least a 10% increase in the relative percentage of one enantiomer versus the other. More preferably, the deracemization reaction provides for a significant increase in one optical isomer over another. Even more preferred, the resulting mixture is substantially enantiomerically pure (90% or greater). Most preferably, the reaction in the presence of an OCIL will produce an enantiomerically pure material (99% of one optional isomer or more).
An example of a deracemization reaction run using an OCIL is:

This is a thermal racimization/deracimization reaction of a chiral vinyl sulfoxide. The reactant exists as a racemate, a 50:50 mixture of enantiomers, at equilibrium. By dissolving this reactant into an OCIL in accordance with the present invention (both N,N-dimethylephedrinium and (−)-N-benzyl-N-methylephedrinium were used successfully) and heating to 50° C.-75° C., followed by cooling to room temperature, deracemization occurred.
Without wishing to be bound by any theory of appreciation, it is believed that the reason the deracemization works so well, is the fact that the sulfoxide to sulfonate rearrangement is reversible and the OCIL more strongly binds to one of the sulfoxide enantiomers than the other, which eventually allows one to convert more of the racemate into one enantiomer. Other factors which are believed to favor one enantiomer over the other include unique ability of OCILs to hydrogen bond through a neighboring alcohol group to functionality in the substrate, further stabilizing one OCIL complex over another. This may be the driving force behind the relatively high enantioselectivity of the photochemical rearrangement discussed earlier.
Another preferred reaction in accordance with the present invention is a reaction wherein a nonchiral or achiral starting material is reacted and converted into a chiral product. Even more preferably, the resulting chiral product is not a racemate. One of the optical isomers will predominate. An example of such a reaction run using an OCIL is:
The starting material was achiral. After a reaction in conventional solvents, a racemic mixture would result. However, when run in an OCIL in accordance with the present invention, ((+)-chloromethyl methyl ether imidazolium IL), with UV applied at about 254 nm at room temperature, one of the optical isomers predominated (60:40). This reaction has also been run in N,N-dimethylephedrinium and resulted in an increase in the percentage of one enantiomer.
Other forms of asymmetric synthesis (producing one optical isomer in greater quantities relative to others) in the presence of an OCIL are a preferred embodiment of this aspect of the invention. A non-limiting list of such reactions was provided above.
Another preferred embodiment in accordance with the present invention involves the use of OCILs as the stationary phase in columns used in liquid chromatography (LC, HPLC) and gas chromatography (“GC”), preferably capillary columns used in gas chromatography. These can be used for separation of optical isomers of chiral materials. Because of their ionic character, OCILs may be used to separate materials which even chiral, but nonionic materials, cannot separate. Any OCIL may be used in accordance with the present invention including PCOCILs and anionic OCILs.
OCILs may be coated onto capillary columns as follows. The entire column is filled with a solution, typically of a cosolvent such as methylene chloride, diethyl ether or pentane) mixed with an OCIL having a concentration appropriate for the deposition of a film of the desired thickness. Typical concentrations of the OCIL is between 0.2-0.3%. This, however, may vary as needed. After filling, one end of the column is sealed, and the other end is connected to a high vacuum pump with an adjustment valve and placed in a water bath. As the volatile non-OCILs slowly evaporate, the solvent front in the capillary retreats back down the fused silica tube leaving a coating of OCILs on the wall. The procedure is continued (with periodic increases in the vacuum to keep the vaporization rate constant) until all the cosolvent has evaporated and, except for an even coating of the OCILs, now called a stationary phase, the column is empty. These columns are then placed into and used in various gas chromatographs in accordance with particular procedures which may be unique to the separation techniques employed and/or to the equipment used.
The synthesis of (1S,2R)-(+)-N,N-dimethylephedrinium trifluoromethanesulfonimide, (1R,2S)-(−)-N,N-dimethylephedrinium trifluoromethanesulfonimide, (1S,2S)-(+)-N,N-dimethylpseudoephedrinium trifluoromethanesulfonimide are described elsewhere.²²Briefly, N-Methylephedrine is dissolved in dichloromethane and equimolar dimethyl sulfate is slowly added. The solvent is removed under reduced pressure and the residue dissolved in water. Addition of an aqueous solution of equimolar of lithium trifluoromethanesulfonimide will lead to the separation of an ionic liquid phase which then is washed three times with water. The final product is heated under reduced pressure at 100° C. to eliminate remaining water.
All capillary columns are coated by static coating method at 40° C. using a 0.25% (w/v) of the IL stationary phase dissolved in dichloromethane. Following the coating process, the coated columns are flushed with dry helium gas overnight and conditioned from 40 to 120° C. at 1° C./min. Column efficiency is tested by naphthalene at 100° C. All columns used will have an efficiency of over 2100 plates/meter.
The racemic test compounds are dissolved in dichloromethane. A Hewlett-Packed model 6890 gas chromatograph and a Hewlett-Packard 6890 series integrator is used for all separations. Split injection and flame ionization detection are utilized with injection and detection temperatures of 250° C. Helium is used as the carrier gas with a flow rate of 1.0 mL/min.

A large number of compounds have been injected into the OCIL columns like those discussed above, which included alcohols, amines, organic acids and oxides. The racemic mixtures listed in Table 1 can be enantiomerically resolved on the OCIL stationary phases. The chromatograms were obtained on an 8 meters (1S,2R)-(+)-N,N-dimethylephedrinium trifluoromethanesulfonimide column.

TABLE 1


Separation of compounds on (1S, 2R)-(+)-N,N-dimethylephedrinium-
bis(trifluoromethanesulfon)imidate column*

			T
#	Compound	Structure	(° C.)	k₁	α


1	Sec-Phenethyl alcohol	120	7.64	1.11

2	1-Phenyl-1-propanol	120	10.1	111

3	1-Phenyl-1-butanol	120	15.3	1.07

4	α-Cyclopropyl- benzyl alcohol	100	37.4	1.03

5	α-Phenyl ethyl amine (TFA derivative)	100	84.1	1.02

6	β-Pinene Oxide	100	12.3	1.03

7	o-Methylphenyl- methyl sulfoxide	140	73.3	1.03

8	o-Chlorophenyl- methyl sulfoxide	140	35.4	1.02

9	o-Bromophenyl- methyl sulfoxide	140	59.2	1.02

10	m-Methylphenyl- methyl sulfoxide	120	241	1.01

11	m-Chlorophenyl- methyl sulfoxide	120	196	1.01

12	m-Bromophenyl- methyl sulfoxide	120	374	1.01

13	trans-1,2- cyclohexandiol	120	21.4	1.10

14	trans-2-Phenyl-1- cyclohexanol	100	100	1.02

*Column length: 8 meters, flow rate: 1 ml/min
k₁is the retention factor for the first enantiomer
α is the ratio of retention times for the enantiomers

All of the compounds listed in Table 1 can form hydrogen bonds with the hydroxyl group on the first chiral center of the chiral ionic liquid stationary phase. A 13 meter (1S,2R)-(+)-N,N-dimethylephedrinium trifluoromethanesulfonimide column was chosen to undergo a TFA derivatization process.²⁴The new column was then tested against all the compounds in Table 1. The experimental results showed that only the sulfoxides can be resolved enantiomerically. Nevertheless, the enantioselectivity became worse. It was also determined that the hydroxyl group on the first chiral center of the chiral stationary phase in this instance was important for the chiral recognition. While the forgoing separations were conducted using gas chromatography, OCILs may be used in the same way in liquid chromatography, including high performance liquid chromatography or HPLC.

EXAMPLE 1

A reaction gives about 3% enantiomeric excess (e.e.) when the N,N-dimethylephedrinium.NTf2 were used as a cosolvent. The reaction is a reduction of methyl phenyl ketone by NaBH₄run at room temperature. The reaction mixture was analyzed by GC using a 20 m Chiraldex™ G-PN column.

REFERENCES

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Claims

1. A chiral cation containing optically enhanced ionic liquid in which at least one enantiomer is enhanced by at least about 2%.

2. The chiral cation containing optically enhanced ionic liquid of claim 1 in which at least one enantiomer is enhanced by at least about 10%.

3. The chiral cation containing optically enhanced ionic liquid of claim 1 in which at least one enantiomer is enhanced by at least about 20%.

4. The chiral cation containing optically enhanced ionic liquid of claim 1 in which at least one enantiomer is substantially optically pure.

5. The chiral cation containing optically enhanced ionic liquid of claim 1 comprising only at least one enantiomerically pure enantiomer.

6. A chiral anion containing optically enhanced ionic liquid which is not a lactate.

7. The chiral anion containing optically enhanced ionic liquid of claim 6 having a melting point of 100° C. or less.

8. A chiral anion containing optically enhanced ionic liquid in which at least one enantiomer is enhanced by at least about 2%.

9. The chiral anion containing optically enhanced ionic liquid of claim 8 in which at least one enantiomer is enhanced by at least about 10%.

10. The chiral anion containing optically enhanced ionic liquid of claim 8 in which at least one enantiomer is enhanced by at least about 20%.

11. The chiral anion containing optically enhanced ionic liquid of claim 8 in which at least one enantiomer is substantially optically pure.

12. The chiral cation containing optically enhanced ionic liquid of claim 8 comprising only at least one enantiomerically pure enantiomer.

13. The asymmetric synthesis of a compound comprising the steps of: conducting a chemical reaction on at least one reactant in the presence of an OCIL to produce a reaction product, and recovering said reaction product; wherein said reaction product is optically active and either only one enantiomer will be present or one enantiomer will be present in an amount which is greater than the other enantiomer of said reaction product.

14. An asymmetric mixture of enantiomers produced in accordance with the process of claim 13.

15. An enantiomerically pure enantiomer produced in accordance with the process of claim 13.

16. A method for deracemization of a racemic compound comprising the steps of: conducting a chemical reaction on at least one racemic reactant in the presence of an OCIL, and producing a reaction product that is optically enhanced.

17. An asymmetric mixture of enantiomers produced in accordance with the process of claim 16.

18. An enantiomerically pure enantiomer produced in accordance with the process of claim 16.

19. A chemical reaction comprising the steps of: mixing, dissolving, dispersing or suspending at least one first reactant in a substantially pure OCIL or in a solvent including a substantially pure OCIL and reacting said at least one first reactant with at least one second reactant, at least one catalyst or said OCIL so as to produce a reaction product which is changed in structure or properties when compared to said at least one first reactant.

20. The chemical reaction of claim 19 wherein said OCIL contains a chiral cation.

21. The chemical reaction of claim 19 wherein said OCIL contains a chiral anion.

22. The reaction product produced in accordance with the process of claim 19.

23. The reaction product produced in accordance with the process of claim 20.

24. The reaction product produced in accordance with the process of claim 21.

25. The reaction product produced in accordance with the process of claim 19 wherein said reaction product is asymmetric.

26. A column for use in chromatography comprising: a column and a stationary phase which is an OCIL associated therewith.

27. The column of claim 26 wherein said column is a capillary and said stationary phase is coated on an inner surface of said capillary.

28. The column of claim 26 wherein said stationary phase is absorbed, adsorbed or coated on a solid support which is packed into said column.

29. A method of separating optical isomers comprising the steps of: mixing, dissolving, dispersing or suspending optical isomers in a mobile phase, introducing said optical isomers into a column that includes at least one OCIL as a stationary phase, and advancing said mobile phase and said optical isomers through said column so as to resolve at least one of said optical isomers.

30. An OCIL having the following structure:

31. An optically enhanced chiral ionic liquid composed of at least one salt comprising both chiral anions and chiral cations.