SEPARATION AND CONCENTRATION OF 2,6-DIMETHYLNAPHTHALENE AND REAGENT FOR SEPARATION AND CONCENTRATION
PURPOSE:To provide a new method for separating the subject compound at low cost by bringing a specified mixture into contact with alpha-cyclodextrin and forming an alpha-cyclodextrin clathrate of 2,6-dimethylnaphthalene. CONSTITUTION:A mixture containing 2,6-dimethylnaphthalene is brought into conta...
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creator | UEMASU ISAMU |
description | PURPOSE:To provide a new method for separating the subject compound at low cost by bringing a specified mixture into contact with alpha-cyclodextrin and forming an alpha-cyclodextrin clathrate of 2,6-dimethylnaphthalene. CONSTITUTION:A mixture containing 2,6-dimethylnaphthalene is brought into contact with a substituted alpha-cyclodextrin synthesized by substituting H of OH in alpha-cyclodextrin with glucosyl, maltosyl, methyl, sulfonic acid, a carboxylalkyl, etc., preferably at 20 to 30 deg.C for several to several ten minutes so as to form an alpha-cyclodextrin clathrate of 2,6-dimethylnaphthalene. The resultant complex is heated at 60 to 70 deg.C so as to liberate 2,6-dimethylnaphthalene and these processes are repeated, thus producing the objective compound of high purity. |
format | Patent |
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CONSTITUTION:A mixture containing 2,6-dimethylnaphthalene is brought into contact with a substituted alpha-cyclodextrin synthesized by substituting H of OH in alpha-cyclodextrin with glucosyl, maltosyl, methyl, sulfonic acid, a carboxylalkyl, etc., preferably at 20 to 30 deg.C for several to several ten minutes so as to form an alpha-cyclodextrin clathrate of 2,6-dimethylnaphthalene. 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CONSTITUTION:A mixture containing 2,6-dimethylnaphthalene is brought into contact with a substituted alpha-cyclodextrin synthesized by substituting H of OH in alpha-cyclodextrin with glucosyl, maltosyl, methyl, sulfonic acid, a carboxylalkyl, etc., preferably at 20 to 30 deg.C for several to several ten minutes so as to form an alpha-cyclodextrin clathrate of 2,6-dimethylnaphthalene. The resultant complex is heated at 60 to 70 deg.C so as to liberate 2,6-dimethylnaphthalene and these processes are repeated, thus producing the objective compound of high purity.</abstract><edition>5</edition><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS APPARATUS THEREFOR CHEMISTRY COMPOSITIONS BASED THEREON DERIVATIVES THEREOF GENERAL METHODS OF ORGANIC CHEMISTRY METALLURGY ORGANIC CHEMISTRY ORGANIC MACROMOLECULAR COMPOUNDS POLYSACCHARIDES THEIR PREPARATION OR CHEMICAL WORKING-UP |
title | SEPARATION AND CONCENTRATION OF 2,6-DIMETHYLNAPHTHALENE AND REAGENT FOR SEPARATION AND CONCENTRATION |
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