Process for the production of carboxylic esters and use of these as plasticizers

Patent metadata

Field	Value
Publication number	US-9776949-B2
Application number	US-201515305932-A
Country	US
Kind code	B2
Filing date	Apr 20, 2015
Priority date	Apr 22, 2014
Publication date	Oct 3, 2017
Grant date	Oct 3, 2017

Abstract

The invention relates to a method for producing carboxylic acid esters by reacting carboxylic acids and/or carboxylic acid anhydrides with at least one alcohol having at least 5 carbon atoms, selected from alkanols and cycloalkanols, in the presence of an ionic liquid and an acidic esterification catalyst. The invention also relates to the use of the thus obtained carboxylic acid esters as a plasticizer or in a plasticizer composition for thermoplastic polymers and elastomers.

First claim

The invention claimed is:

1. A process for the production of a carboxylic ester, comprising:
reacting at least one carboxylic acid and/or at least one carboxylic anhydride, selected from aromatic mono-, di-, tri-, or tetracarboxylic acids, aliphatic mono- and dicarboxylic acids, hydroxycarboxylic acids, alicyclic mono-, di-, tri-, and tetracarboxylic acids, heterocyclic dicarboxylic acids, the anhydrides of the abovementioned carboxylic acids, and mixtures thereof,
with
at least one alcohol R l —OH, in which R 1 is selected among unbranched and branched saturated C 5 -C 13 -alkyl moieties,
with the proviso that the reaction takes place
in the presence of at least one ionic liquid which is selected from among salts of the general formula (Ia),

in which
radicals R 2 and R 3 , independently of one another, are hydrogen, unsubstituted or substituted alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl or heteroaryl,
radicals R 4 , R 5 , and R 6 , independently of one another, are hydrogen, unsubstituted or substituted alkyl, alkenyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, aryl, heteroaryl or alkoxy,
and
R c is alkyl, cycloalkyl or aryl, where aryl may be substituted by 1, 2 or 3 alkyl radicals,
in the presence of at least one catalyst selected among organic sulfonic acids, wherein the at least one catalyst is not covalently attached to the ionic liquid of the general formula (Ia), and
with distillative removal, in the form of an azeotropic mixture with the alcohol R 1 —OH used, of at least one portion of the water formed during the reaction,
where at least to some extent the alcohol R 1 —OH removed by distillation is returned to the reaction system.

2. The process according to claim 1 , wherein the reaction takes place with supply to the reaction system of a gas which is inert under the reaction conditions.

3. The process according to claim 1 , wherein the reaction takes place at a reaction mixture temperature of 60 -250° C.

4. The process according to claim 1 , wherein the anion of the at least one ionic liquid corresponds to the deprotonated form of the organic sulfonic acid used as catalyst.

5. The process according to claim 2 , wherein the reaction of at least one carboxylic acid and/or of at least one carboxylic anhydride and of at least one alcohol R 1 —OH is carried out in at least one reactor, where the inert gas is passed into the at least one reactor below the liquid surface, and the inert gas is bubbled through the reaction mixture.

6. The process according to claim 2 , where the reaction takes place in a cascade made of at least two reactors.

7. The process according to claim 6 , where the inert gas is introduced at least into the first reactor of the cascade.

8. The process according to claim 1 , wherein the reaction is carried out continuously.

9. The process according to claim 1 , wherein the radical R 1 is n-octyl, 2-ethylhexyl, n-nonyl, isononyl, isodecyl, 2-propylheptyl, n-undecyl, or isoundecyl.

10. The process according to claim 1 , wherein 2-ethylhexanol is used as alcohol R 1 —OH.

11. The process according to claim 1 , wherein the at least one carboxylic acid is at least one of benzoic acid, benzoic anhydride, phthalic acid, phthalic anhydride, isophthalic acid, terephthalic acid, trimellitic acid, trimellitic anhydride, pyromellitic acid, and pyromellitic dianhydride.

12. The process according to claim 1 , for the production of bis(2-ethylhexyl) terephthalate by reaction of terephthalic acid with 2-ethylhexanol.

13. The process according to claim 1 , wherein the at least one alcohol R 1 —OH is present in a 1.01- to 2.0-fold molar excess, based on the carboxylic acid equivalents of the carboxylic acid material used.

14. The process according to claim 1 , wherein the catalyst comprises at least one alkylsulfonic acid.

15. The process according to claim 1 , wherein methanesulfonic acid is used as catalyst.

16. The process according to claim 1 , wherein the amount used of the catalyst, based on the number of the carboxylic acid groups to be reacted, is from 0.5 to 5 mol %.

17. The process according to claim 1 , wherein the fraction of the ionic liquid in the reaction mixture is from 1 to 50% by weight, based on the total weight of the reaction mixture.

18. The process according to claim 1 , wherein, after the reaction has ended, an ionic fraction which comprises the ionic liquid, the at least one catalyst and also any unreacted carboxylic acid and/or unreacted carboxylic anhydride is removed from the reaction mixture and used again for further esterification reactions.

19. The process according to claim 1 , wherein the catalyst consists of at least one alkylsulfonic acid.

Assignees

• Basf Se

Inventors

• Kaller Martin
• Koch Michael

Classifications

• Y02P20/582

  Recycling of unreacted starting or intermediate materials · CPC title

• C08K5/10

  Esters; Ether-esters · CPC title

• C08K5/0016

  Plasticisers · CPC title

• C07D233/58

  with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring nitrogen atoms · CPC title

• C07C69/82

  Terephthalic acid esters · CPC title