US2023357116A1PendingUtilityA1

Alcohols Production

Assignee: SCION Holdings LLCPriority: Jun 5, 2020Filed: May 17, 2023Published: Nov 9, 2023
Est. expiryJun 5, 2040(~13.9 yrs left)· nominal 20-yr term from priority
C07C 45/505B01J 31/2495B01J 31/2404B01J 31/185C07C 5/2593C07C 2531/24B01J 2231/52B01J 2531/822B01J 2231/321C07C 45/50C07C 2523/46B01J 25/02
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Claims

Abstract

A process for producing branched alcohols through isomerization, hydroformylation and hydrogenation.

Claims

exact text as granted — not AI-modified
1 . A process, comprising the steps of:
 providing CO and H2;   providing a first catalyst which is an organometallic complex of rhodium and one type of an organophosphorus ligand or an organometallic complex of rhodium and more than one type of an organophosphorus ligand;   providing a linear alpha olefin;   isomerizing said linear alpha olefin by said first catalyst in the presence of CO and H2 at a first pressure to produce an isomerized olefin; and   hydroformylating said isomerized olefin by said first catalyst in the presence of CO and H2 at a second pressure different from said first pressure to produce a branched aldehyde.   
     
     
         2 . The process according to  claim 1 , wherein said branched aldehyde is a 2-alkyl branched aldehyde. 
     
     
         3 . The process according to  claim 1 , wherein said linear alpha olefin is a C4-C36 linear alpha olefin. 
     
     
         4 . The process according to  claim 1 , wherein said branched aldehyde produced from a C4-C36 linear alpha olefin comprises a C5-C37 branched aldehyde. 
     
     
         5 . The process according to  claim 1 , wherein said linear alpha olefin is a 1-Butene and said branched aldehyde comprises a branched Pentanal. 
     
     
         6 . The process according to  claim 1 , wherein said linear alpha olefin is a 1-Hexene and said branched aldehyde comprises a branched Heptanal. 
     
     
         7 . The process according to  claim 1 , wherein said linear alpha olefin is a 1-Octene and said branched aldehyde comprises a branched Nonanal. 
     
     
         8 . The process according to  claim 1 , wherein said linear alpha olefin is a 1-Decene and said branched aldehyde comprises a branched Undecanal. 
     
     
         9 . The process according to  claim 1 , wherein said linear alpha olefin is a 1-Dodecene and said branched aldehyde comprises a branched Tridecanal. 
     
     
         10 . The process according to  claim 1 , wherein said linear alpha olefin is a 1-Tetradecene and said branched aldehyde comprises a branched Pentadecanal. 
     
     
         11 . The process according to  claim 1 , wherein said linear alpha olefin is a 1-Hexadecene and said branched aldehyde comprises a branched Heptadecanal. 
     
     
         12 . The process according to  claim 1 , wherein said linear alpha olefin is a 1-Octadecene and said branched aldehyde comprises a branched Nonadecanal. 
     
     
         13 . The process according to  claim 1 , wherein the organophosphorous ligand can be a phosphine. 
     
     
         14 . The process according to  claim 1 , wherein the phosphine ligand can be triphenylphosphine. 
     
     
         15 . The process according to  claim 1 , wherein the organophosphorous ligand can be a phosphite. 
     
     
         16 . The process according to  claim 1 , wherein the phosphite ligand can be tris (2, 4-di-t-butylphenyl) phosphite. 
     
     
         17 . The process according to  claim 1 , wherein a mixture of organophosphorous ligands of different types can be used, such as a mixture of a phosphine and a phosphite. 
     
     
         18 . The process according to  claim 1 , wherein a mixture of organophosphorous ligands of different types can be a mixture of triphenylphosphine and tris (2, 4-di-t-butylphenyl) phosphite. 
     
     
         19 . The process according to  claim 1 , wherein said first catalyst is formed when the molar ratio of phosphorous to rhodium in a range of 1:1 to 1000:1.

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