IP Library Granted Patent US 7,002,053
Granted Patent B2
US 7,002,053 · App. 10/467,844 · Granted Feb 21, 2006

Method for preparing high-purity diisobutene

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Quick Facts
Patent No.
US 7,002,053
App. No.
10/467,844
Granted
Feb 21, 2006
Kind
B2
Abstract

The invention relates to a process for preparing high-purity diisobutene by reaction of isobutene or isobutene-containing hydrocarbon mixtures over a solid acidic ion-exchange resin containing sulfonic acid groups whose protons have been partly replaced by metal ions and to the use of the diisobutene.

Claims (15)

1. A process for preparing high-purity diisobutene comprising:

reacting isobutene or isobutene-containing hydrocarbon mixtures in the presence of a solid acidic ion-exchange resin containing sulfonic acid groups whose protons have been partly replaced by metal ions.

2. The process as claimed in claim 1 , wherein from 30 to 90% of the protons have been replaced by metal ions.

3. The process as claimed in claim 1 , wherein from 50 to 80% of the protons have been replaced by metal ions.

4. The process as claimed in claim 1 , wherein the metal ions are alkali metal ions.

5. The process as claimed in claim 1 , wherein the metal ions are sodium ions.

6. The process as claimed in claim 1 , wherein the reaction is carried out at from 20 to 120° C.

7. The process as claimed in claim 6 , wherein the reaction is carried out at from 40 to 100° C.

8. The process as claimed in claim 1 , wherein the reaction is carried out in a liquid phase in a pressure range of from 5 to 40 bar.

9. A method of preparing 3,5,5-trimethyihexanoic acid comprising hydroformylation and subsequent oxidation of the diisobutene prepared according to the process of claim 1 , wherein said diisobutene is part of a mixture comprising a C 8 fraction and higher oligomers, wherein the diisobutene content is over 99.7% of said C 8 fraction.

10. A method of preparing 3,5,5-trimethylhexanol comprising hydroformylation and subsequent hydrogenation of the diisobutene prepared according to the process of claim 1 , wherein said diisobutene is part of a mixture comprising a C 8 fraction and higher oligomers, wherein the diisobutene content is over 99.7% of said C 8 fraction.

11. A method of alkylating phenols and/or aromatic amines comprising reacting the diisobutene prepared according to the process of claim 1 with phenols and/or aromatic amines, wherein said diisobutene is part of a mixture comprising a C 8 fraction and higher oligomers, wherein the diisobutene content is over 99.7% of said C 8 fraction.

12. A method of preparing 3,5,5-trimethylhexanoic acid comprising carrying out the process of claim 1 , followed by hydroformylation and subsequent oxidation.

13. A method of preparing 3,5,5-trimethyihexanol comprising carrying out the process of claim 1 , followed by hydroformylation and subsequent hydrogenation.

14. A method of alkylating phenols and/or aromatic amines comprising carrying out the process of claim 1 , followed by reacting with phenols and/or aromatic amines.

Assignments (3)
MERGER Recorded Feb 26, 2014
From: EVONIK OXENO GMBH
To: EVONIK DEGUSSA GMBH
Reel/Frame 032335/0453 →
CHANGE OF NAME Recorded Feb 25, 2010
From: OXENO OLEFINCHEMIE GMBH
To: EVONIK OXENO GMBH
Reel/Frame 024006/0287 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 11, 2003
From: NIERLICH, FRANZ; KERKER, LOTHAR; PETERS, UDO; BUESCHKEN, WILFRIED; BECKMANN, ANDREAS
To: OXENO OLEFINCHEMIE GMBH
Reel/Frame 014781/0399 →