Organic compounds -- part of the class 532-570 series – Organic compounds – Nitriles
Reexamination Certificate
2000-12-29
2002-08-27
McKane, Joseph K. (Department: 1626)
Organic compounds -- part of the class 532-570 series
Organic compounds
Nitriles
Reexamination Certificate
active
06441217
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to a novel ferulic acid derivative and further to a liquid crystal material, a cation detecting element, an anion detecting element, an ion conducting material and an electrolyte, each using the ferulic acid derivative.
2. Description of the Prior Art
Phenols have heretofore been finding utility as an anti-oxidizing agent for addition to foodstuffs. In recent years, polyphenols have been attracting further attention on account of their ability to manifest an effect of repressing carcinogenesis. Furthermore, a group of researchers in Wakayama prefecture of Japan has developed a method for extracting and isolating ferulic acid, one of phenol derivatives, from the waste oil of rice bran inexpensively in a large amount. Therefore, the feasibility of commercializing the ferulic acid for utility in biochemical applications has been attracting attention from various quarters.
At the present stage, however, uses which can be expected to create large demands for the ferulic acid so produced have not been found. If a demand that can promises an effective utility of the ferulic acid is found, the waste oil of rice bran, which has heretofore been treated as an industrial waste and consequently fated to be discarded, can be effectively utilized instead. As a result, the amount of industrial waste will be decreased and the development of inexpensive commercial products will be hoped for.
In view of the above, an object of this invention is to provide a novel ferulic acid derivative produced from ferulic acid as the raw material and exhibiting characteristic properties expected to find extensive utility and generate a great demand therefor. Another object of the invention is to provide a liquid crystal material, a metal ion-detecting element, an ion conducting material and an electrolyte which are formed respectively of the derivative.
To accomplish these objects, the present inventors have studied the design of a novel liquid crystal material with a view to effectively utilizing the ferulic acid. Specifically, they have tried design and configuration of an ion transfer material of a new type which, by introducing a group capable of coordinating with a metal ion to a hydroxyl group of ferulic acid, can utilize the two-dimensional state of molecular aggregation to be formed by liquid crystal molecules in the state of liquid crystal.
SUMMARY OF THE INVENTION
A ferulic acid derivative according to this invention is a compound represented by the following general formula:
wherein R denotes a polyethylene glycol group, a crown ether group or an azacrown ether group.
A liquid crystal material according to this invention is a compound represented by the following general formula:
wherein R denotes a polyethylene glycol group, a crown ether group or an azacrown ether group.
A liquid crystal material according to this invention is formed by the coordination of at least one member selected from the group consisting of alkali metal ions, alkaline earth metal ions, and transition metal ions with a compound represented by the following general formula:
wherein R denotes a polyethylene glycol group, a crown ether group or an azacrown ether group.
This invention embraces a detecting element formed of the ferulic acid derivative mentioned above and intended to detect at least one species of cation selected from the group consisting of alkali metal ions, alkaline earth metal ions and transition metal ions.
This invention further embraces an anion detecting element formed by coordinating at least one member selected from the group consisting of alkali metal ions, alkaline earth metal ions and transition metal ions with the ferulic acid derivative mentioned above.
This invention also embraces an ion conducting material formed by coordinating at least one member selected from the group consisting of alkali metal ions, alkaline earth metal ions and transition metal ions with the ferulic acid derivative mentioned above.
This invention also embraces an electrolyte formed by coordinating at least one member selected from the group consisting of alkali metal ions, alkaline earth metal ions and transition metal ions with the ferulic acid derivative mentioned above.
The ferulic acid derivative or the liquid crystal material contemplated by this invention is a useful element applicable as a metal sensing material, an ion conducting material and an electrolyte.
The ferulic acid derivative of this invention, in a state not coordinated with any ion, is useful as a sensor (detecting element) for a cation (a metal ion, for example) and, in a state coordinated with a cation (a metal ion, for example), is useful as an anion sensor (anion detecting element).
DESCRIPTION OF THE PREFERRED EMBODIMENT
The general formula of the ferulic acid derivative according to this invention is as shown below.
As a concrete example of the polyethylene glycol group denoted by R in the general formula of the ferulic add derivative, the group which is represented by the formula, —CH
2
CH
2
(OCH
2
CH
2
)
n
—OH (wherein n denotes an integer of 1 to 10), may be cited. In the formula, n denotes an integer of 1 to 10, preferably 1 to 6.
The crown ether group denoted by R in the ferulic acid derivative does not need to be particularly discriminated but is only required to be a group having a crown ether moiety. As preferred examples of the crown ether group, there may be cited the groups in which the number of oxygen atoms forming rings such as 12-crown-4, 15-crown-5, 18-crown-6, 24-crown-8, dibenzo 18-crown-6, dibenzo 24-crown-8, cryptand [2.2] and cryptand [2.2.2] is in the range of 3 to 8, the adjoining oxygen atoms have a crown ether structure concatenated with methylene, 1,2-phenylene or propylene, and the crown ether is connected either directly to the methylene, 1,2-phenylene or propylene forming the ring, or optionally via a spacer such as methylene or propylene to the phenolic hydroxyl group of a ferulic acid.
As concrete examples of the azacrown ether group represented by R in the ferulic acid derivative, the groups in which the oxygen atoms of the crown ether group are displaced with nitrogen atoms may be cited.
The ferulic acid derivative (I) can be produced, for example, in accordance with the following formula of reaction process.
<Formula of Reaction Process>
wherein R has the same definition as mentioned above, X denotes a leaving group, and R′ denotes a methyl group, an ethyl group, a propyl group or a butyl group.
The ferulic acid (1) is left reacting in an alcohol such as methanol, ethanol, propanol or butanol with sulfuric acid at a temperature in the range of from normal room temperature to the refluxing temperature of the alcohol for a period in the range of 30 minutes to five hours to obtain an ester (2).
Then, one mol of the ester (2) is caused to react with about 1 to 2 mols of R-X (3) as refluxed in a solvent (such as 2-butanone) in the presence of a base such as potassium carbonate for a period in the range of 10 to 96 hours to effect introduction of the R group. Subsequently, the compound consequently obtained is left reacting in a solvent such as 2-butanone containing an aqueous 5% NaOH solution at a temperature approximating closely to normal room temperature for a period in the range of 1 to 24 hours to effect hydrolysis of ester and obtain a ferulic acid derivative (4) having the R group introduced.
One mol of the ferulic acid derivative (4), and about 1 to 2 mols of 4-hydroxy-4′-cyanobiphenyl (5), about 1 to 2 mols of a condensation agent such as dicydohexyl carbodiimide (DCC) and a catalytic amount (about 10 mol %, for example) of dimethyl aminopyridine added thereto are left reacting in a solvent such as dichloromethane at a temperature in the range of from the temperature of the ice-cold water to the approximate temperature enabling the solvent to be refluxed for a period in the range of 1 to 24 hours to obtain the ferulic acid derivative (I).
As concrete examples of the leaving group denoted by X,
Monobe Hirosato
Shimizu Yo
Sugino Takushi
Agency of Industrial Science & Technology, Ministry of Internati
McKane Joseph K.
Oblon & Spivak, McClelland, Maier & Neustadt P.C.
Sackey Ebenezer
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