The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 27, 2018

Filed:

Feb. 01, 2018
Applicant:

Exxonmobil Research and Engineering Company, Annandale, NJ (US);

Inventors:

Michael P. Lanci, Flemington, NJ (US);

Changyub Paek, Bridgewater, NJ (US);

Catherine M. Dorsi, Houston, TX (US);

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07C 2/74 (2006.01); C07C 5/42 (2006.01); C07C 7/12 (2006.01); C07C 7/13 (2006.01); C07C 5/367 (2006.01); C07C 5/27 (2006.01); C07C 5/10 (2006.01); C07C 2/66 (2006.01);
U.S. Cl.
CPC ...
C07C 2/74 (2013.01); C07C 2/66 (2013.01); C07C 5/10 (2013.01); C07C 5/2732 (2013.01); C07C 5/367 (2013.01);
Abstract

In a process for producing one or more 3,3'-, 3,4′- and 4,4′-dimethyl biphenyl isomers, a feed comprising toluene is contacted with hydrogen in the presence of a hydroalkylation catalyst under conditions effective to produce a hydroalkylation reaction product comprising (methylcyclohexyl)toluenes. At least part of the hydroalkylation reaction product is dehydrogenated in the presence of a dehydrogenation catalyst under conditions effective to produce a dehydrogenation reaction product comprising a mixture of dimethyl biphenyl isomers. The dehydrogenation reaction product is then separated into at least a first stream containing one or more 3,3′-, 3,4′- and 4,4′-dimethyl biphenyl isomers and at least one second stream comprising one or more 2,X′-dimethyl biphenyl isomers (where X is 2, 3, or 4). The 3,3′-, 3,4′- and 4,4′-dimethyl biphenyl isomers are then separated utilizing selective adsorption.


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