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:
Apr. 19, 2022

Filed:

Mar. 30, 2018
Applicant:

University of Virginia Patent Foundation, Charlottesville, VA (US);

Inventors:

William Schinski, San Rafael, CA (US);

Alan Goldman, Highland Park, NJ (US);

Thomas B. Gunnoe, Palmyra, VA (US);

Michael S. Webster-Gardiner, Mims, FL (US);

Nichole Schwartz, Charlottesville, VA (US);

Assignee:

University of Virginia Patent Foundation, Charlottesville, VA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07C 2/66 (2006.01); B01J 21/04 (2006.01); B01J 21/08 (2006.01); B01J 23/42 (2006.01); B01J 23/46 (2006.01); B01J 29/44 (2006.01); B01J 31/18 (2006.01); B01J 31/22 (2006.01); C07C 5/333 (2006.01); C07C 5/41 (2006.01);
U.S. Cl.
CPC ...
C07C 2/66 (2013.01); B01J 21/04 (2013.01); B01J 21/08 (2013.01); B01J 23/42 (2013.01); B01J 23/464 (2013.01); B01J 29/44 (2013.01); B01J 31/183 (2013.01); B01J 31/2226 (2013.01); B01J 31/2291 (2013.01); C07C 5/333 (2013.01); C07C 5/41 (2013.01); B01J 2231/32 (2013.01); B01J 2531/0244 (2013.01); B01J 2531/822 (2013.01); B01J 2531/827 (2013.01); C07C 2521/04 (2013.01); C07C 2521/08 (2013.01); C07C 2523/46 (2013.01); C07C 2529/44 (2013.01); C07C 2531/22 (2013.01);
Abstract

Catalytic methods for synthesis of super linear alkenyl arenes and alkyl arenes are provided. The methods are capable of synthesizing super linear alkyl and alkenyl arenes from simple arene and olefin starting materials and with high selectivity for linear coupling. Methods are also provided for making a 2,6-dimethylnapthalene (DMN) or 2,6-methylethylnapthalene (MEN).


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