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:
Jan. 30, 2024

Filed:

May. 26, 2022
Applicant:

Chevron Phillips Chemical Company Lp, The Woodlands, TX (US);

Inventors:

Brooke L. Small, Kingwood, TX (US);

Michael S. Webster-Gardiner, Humble, TX (US);

Assignee:

Chevron Phillips Chemical Company LP, The Woodlands, TX (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07C 5/03 (2006.01); C07C 45/50 (2006.01); C07C 1/207 (2006.01); B01J 31/28 (2006.01); B01J 23/44 (2006.01); C07C 1/24 (2006.01);
U.S. Cl.
CPC ...
C07C 5/03 (2013.01); B01J 23/44 (2013.01); B01J 31/28 (2013.01); C07C 1/2076 (2013.01); C07C 1/24 (2013.01); C07C 45/505 (2013.01); C07C 2523/44 (2013.01);
Abstract

An alpha olefin synthesis process includes (i) subjecting a first normal alpha olefin to hydroformylation in the presence of carbon monoxide and hydrogen to form a first linear aldehyde, (ii) subjecting the first linear aldehyde to decarbonylative olefination to form a linear internal olefin, (iii) subjecting the linear internal olefin to isomerization-hydroformylation in the presence of carbon monoxide and hydrogen to form a second linear aldehyde, and (iv) subjecting the second linear aldehyde to hydrogenation to form a linear alcohol followed by dehydration to form a second normal alpha olefin, or subjecting the second linear aldehyde to combined hydrogenation-dehydration in a single step to form a second normal alpha olefin. Using this process, for example, ethylene can be converted to 1-hexene, and 1-butene can be converted to 1-decene.


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