Occidental Chemical Corporation

Viesturs Lesins

David Y Tang

Mark E Lindrose

Arthur H Morth

Frank P Bermel

William L Rueter

Michael J Fifolt

William S Derwin

Hang-Chang Bobby Chen

Habib Hichri

Dean R Lagerwall

Pravin M Khandare

Mark F Lechner

Christopher C Sommer

Disclosed is a method of separating the meta isomer of a haloalkylbenzene having the general formula

Reducing meta content of isomeric mixtures of halo substituted alkylbenzenes

Disclosed is a method of making high purity 2,4- and 3,4-dichlorotoluene from parachlorotoluene that contains some metachlorotoluene. About 0.0001 to about 5 wt % of a Friedel-Crafts catalyst and about 0.5 to about 10 equivalents of a brominating agent are added to the parachlorotoluene. The metachlorotoluene is brominated, but most of the parachlorotoluene is not brominated. Without separating the brominated products from the unbrominated products, about 0.5 to about 1.5 equivalents of a chlorinating agent are added, whereby only the unbrominated products (i.e., the parachlorotoluene) are chlorinated. The resulting 2,4-dichlorotoluene and 3,4-dichlorotoluene can be separated by distillation.

Method of making high purity 2,4- and 3,4-dichlorotoluene

Disclosed is a method of separating the meta isomer of a halotoluene having the general formula ##STR1## from a mixture with at least one other isomer, where X is Cl or Br. About 0.0001 to about 5 wt % of a Friedel-Crafts catalyst is added to the mixture and the mixture is exposed to a brominating agent which preferentially brominates the meta isomer. The mixture is then heated at a temperature above the boiling point of the other isomers but below the boiling point of the brominated meta isomer.

Reducing meta content of isomeric mixtures of halo substituted toluenes

Disclosed is method of sulfodechlorinating an aromatic compound. A composition is prepared of (1) an aromatic compound having the general formula ##STR1## Where R is CHO or COOH and n is 1 to 3, (2) an alkali metal or alkaline earth metal sulfite or bisulfite in an amount stoichiometric to about 20 mole % in excess of stoichiometric, (3) water in an amount sufficient to form a solution of the sulfite or bisulfite, and (4) sufficient base to raise the pH of the composition to about 10 to about 14. The composition is heated at about 150 to about 200.degree. C. No catalyst is present in the composition.

Sulfodechlorinating aromatic compounds

Disclosed is a method of making oxydiphthalic anhydride from oxydiphthalic acid. The oxydiphthalic acid is mixed with an organic liquid that codistills with water and the resulting slurry is heated to the boiling point of the slurry to remove any water. About 1 to about 4 moles of acetic anhydride per mole of oxydiphthalic acid are added to the slurry and the slurry is heated to a temperature between 50.degree. and 160.degree. C. until the oxydiphthalic acid content thereof is less than 0.1 weight percent. The slurry is filtered and the filter cake is heated to a temperature between about 180.degree. C. and below its melting point for about 12 to about 24 hours.

Method of making oxydiphthalic anhydride

A process for the preparation of purified oxydiphthalic acid from impure oxydiphthalic anhydride, by treating with a mixture of water and propionic acid or butyric acid to produce oxydiphthalic acid. The acid may be treated to reform oxydiphthalic anhydride. The most effective composition range for the acid-water mixture is from about 25% acid to 75% acid.

Growing community of inventors

Buffalo, NY, United States of America

Viesturs Lesins