Process for the preparation of sorbic acid

Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acids and salts thereof

Reexamination Certificate

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Reexamination Certificate

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06437182

ABSTRACT:

This application is the national phase under 35 U.S.C. §371 of PCT International Application No. PCT/JP99/05123 which has an International filing date of Sep. 21, 1999,which designated the United States of America.
TECHNICAL FIELD
The present invention relates to a process for producing sorbic acid which is useful as, for example, food additives. Particularly, the invention relates to a process for producing sorbic acid by decomposition of a polyester obtained from ketene and crotonaldehyde.
BACKGROUND ART
As processes for the commercial production of sorbic acid, processes are known which include the step of hydrolyzing a polyester in the presence of an acid, which polyester is obtained by a reaction of ketene with crotonaldehyde. For example, Japanese Examined Patent Application Publication No. 44-26646 discloses a process for producing sorbic acid. The process includes the steps of reacting ketene with crotonaldehyde in the presence of a catalyst to yield a reaction mixture, heating the reaction mixture under reduced pressure to remove unreacted crotonaldehyde and by-products of the reaction by distillation to yield a polyester containing the catalyst, decomposing the polyester with hydrochloric acid to yield a reaction mixture, and cooling the reaction mixture to yield sorbic acid.
In such processes for producing sorbic acid by hydrolyzing the polyester with an acid, a purified sorbic acid is generally obtained by preparing a reaction mixture slurry by the hydrolysis of the polyester in the presence of an acid, subjecting the reaction mixture slurry to filtration or another solid-liquid separation operation to yield a crude sorbic acid as a solid, and subjecting the crude sorbic acid to a purification process such as treatment with active carbon or crystallization. The reaction mixture slurry contains tar substances by-produced in the reaction. In the solid-liquid separation, some of the tar substances migrate to liquid portions, but others adhere to a surface of sorbic acid and migrate to solid portions. To obtain a highly purified sorbic acid having a satisfactory hue, loads on the subsequent purification process such as treatment with active carbon must be increased or a combination of several complicated purification processes must be employed.
The Japanese Examined Patent Application Publication No. 44-26646 discloses a process for producing sorbic acid. The process includes the steps of preparing a polyester from ketene and crotonaldehyde, and decomposing the polyester with hydrochloric acid having a concentration of 35% by weight or more at temperatures ranging from room temperature to around the boiling point of the hydrochloric acid used. In an example described in this publication, a crystalline sorbic acid is obtained by cooling a reaction mixture, separating a crude sorbic acid by filtration, washing the crude sorbic acid with water, putting the washed crude sorbic acid into water, heating and dissolving the mixture to yield a solution, adding activated carbon to the solution, boiling the mixture, and filtering the mixture while heating, and gradually cooling the resulting filtrate to yield a crystalline sorbic acid. Japanese Unexamined Patent Application Publication No. 9-227447 discloses a process for producing sorbic acid. The process includes the step of performing isomerization at a specific temperature after the completion of heat generation in the hydrolysis of the polyester. In an example described in this publication, a crude sorbic acid is obtained by cooling a reaction mixture to 25° C. and filtrating the cooled reaction mixture under suction. Japanese Unexamined Patent Application Publication No. 10-95745 discloses a process for producing sorbic acid, including the step of hydrolyzing the polyester with a mineral acid in the presence of a saturated fatty acid. An example shown in this publication describes that a crude sorbic acid was obtained by cooling a reaction mixture to 20° C. and filtrating the cooled reaction mixture under suction.
However, when a hydrolysis reaction mixture of the polyester is cooled to about 20° C. to 25° C. and is then filtered as in the above processes, such by-product tar substances are highly viscous, and large portions of the tar substances adhere to sorbic acid and migrate to solid portions. This markedly increases loads on subsequent sorbic acid purification process such as treatment with active carbon.
Such a decomposition reaction mixture of the polyester contains an acid used in the reaction. The acid will corrode apparatus and instruments in the purification process and should be preferably removed completely as soon as possible.
DISCLOSURE OF INVENTION
Accordingly, an object of the invention is to provide a process for producing sorbic acid, which is capable of easily and efficiently removing tar substances by-produced in a reaction and is capable of mitigating loads on a purification process.
Another object of the invention is to provide a process for efficiently producing a highly purified sorbic acid having a satisfactory hue.
It is a further object of the invention to provide a process for producing sorbic acid, which is capable of efficiently removing not only tar substances but also the acid used in a reaction.
The present inventors made intensive investigations to achieve the above objects, and found that tar substances can be efficiently removed by subjecting a decomposition reaction mixture of the polyester to solid-liquid separation at temperatures in a specific range.
Specifically, the invention provides a process for producing sorbic acid by hydrolysis of a polyester in the presence of an acid, which polyester is obtained from ketene and crotonaldehyde. The process includes the step of subjecting a reaction mixture formed by decomposition of the polyester to solid-liquid separation at temperatures ranging from 30° C. to 60° C. to yield sorbic acid as a solid.
BEST MODE FOR CARRYING OUT THE INVENTION
According to the invention, a polyester obtained from ketene and crotonaldehyde is hydrolized in the presence of an acid to yield sorbic acid. The polyester is generally shown by the following formula (1):
In the above formula, R is an acetoxy group or a hydroxyl group, and n denotes an integer of 2 or more (e.g., about 3 to 40).
The polyester can be obtained by conventional or known processes. For example, the polyester is obtained by reacting ketene with crotonaldehyde in the presence of a catalyst and in the absence of or in the presence of an inert solvent. Such catalysts include, but are not limited to, simple substances or compounds of manganese, cobalt, nickel, zinc, cadmium, and other transition metals; and pyridine, picoline, and other nitrogen-containing basic compounds. Examples of the compounds of the transition metals are oxides; salts of acetic acid, salts of isobutyric acid, salts of isovaleric acid, and salts of other organic acids; salts of sulfuric acid, salts of nitric acid, and salts of other inorganic acids; chlorides and other halides; acetylacetone complex salts, and other complex salts and complexes. Each of these catalysts can be used alone or in combination. The amount of the catalyst differs according to the type of the catalyst, but is generally about 0.1 to 10% by weight relative to the weight of ketene.
The reaction of ketene with crotonaldehyde is performed at a temperature of, for example, about 20° C. to 100° C., and preferably about 25° C. to 80° C.
A reaction mixture containing the polyester obtained through the reaction of ketene with crotonaldehyde is usually distilled to remove unreacted crotonaldehyde and low boiling impurities, and is then subjected to a hydrolysis reaction with an acid.
Acids for use in hydrolysis of the polyester include mineral acids such as hydrochloric acid and sulfuric acid. The hydrolysis of the polyester is frequently performed in hydrochloric acid. When the polyester is hydrolyzed with hydrochloric acid, the concentration of hydrochloric acid is, for example, about 15 to 40% by weight and more preferably about 23 to 36% by weight. An ext

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