22768-18-9Relevant academic research and scientific papers
Isononylamines from 2-Ethylhexanol, Processes for Their Preparation, and Their Use
-
Paragraph 0056-0057, (2015/06/10)
Process for preparing isononylamines starting out from 2-ethylhexanol, characterized in that (a) 2-ethylhexanol is dehydrated in the presence of a catalyst to form octene; (b) the octene obtained in step a) is reacted with carbon monoxide and hydrogen in the presence of a transition metal compound of group VIII of the Periodic Table of the Elements to form isononanal; and (c) the isononanal obtained in step b) is converted into isononylamines.
Vinyl Esters of Isononanoic Acid Starting from 2-Ethyl Hexanol, Methods for the Production Thereof and Use Thereof
-
Paragraph 0075-0077, (2015/06/24)
Process for preparing the vinyl ester of isononanoic acid starting out from 2-ethylhexanol, characterized in that (a) 2-ethylhexanol is dehydrated in the presence of a catalyst to form octene; (b) the octene obtained in step a) is converted into an isononanoic acid having one more carbon atom; and (c) the isononanoic acid obtained in step b) is converted into the corresponding vinyl ester.
Method for Producing Isononanoic Acid Esters, Starting from 2-Ethyl Hexanol
-
Paragraph 0074-0076, (2015/06/17)
A Process for preparing carboxylic esters of a mixture of structurally branched C9 monocarboxylic acids proceeding from 2-ethylhexanol is characterized in that (a) 2-ethylhexanol is dehydrated to an octene mixture in the presence of a catalyst; (b) the octene mixture obtained in step a) is reacted in the presence of a transition metal compound of group VIII of the periodic table of the elements with carbon monoxide and hydrogen to give a mixture of isomeric isononanals; (c) the mixture of isomeric isononanals obtained in step b) is oxidized to a mixture of structurally branched C9 monocarboxylic acids; and (d) the mixture of structurally branched C9 monocarboxylic acids obtained in step c) is reacted with alcohols to give carboxylic esters.
Method for Producing Isononanoic Acids from 2-Ethyl Hexanol
-
Paragraph 0062-0063, (2015/07/15)
Process for preparing isononanoic acid proceeding from 2-ethylhexanol, characterized in that (a) 2-ethylhexanol is dehydrated to octene in the presence of a catalyst; (b) the octene obtained in step a) is reacted in the presence of a transition metal compound of group VIII of the periodic table of the elements with carbon monoxide and hydrogen to give isononanal; and (c) the isononanal obtained in step b) is oxidized to isononanoic acid.
TURBINE AND DIESEL FUELS AND METHODS FOR MAKING THE SAME
-
Paragraph 0065; 0066, (2013/11/18)
A process for making diesel and turbine fuels includes providing an amount of one or more branched olefins and adding active heterogeneous acid catalyst(s) to the branched olefins to produce a mixture, which can be solvent-free. The process further includes heating the solvent-free mixture to a temperature greater than about 80°C for a sufficient time to produce a dimers/catalyst mixture, removing the catalysts from the dimers/catalyst mixture, and adding hydrogenation catalyst(s) to the dimers under hydrogen atmosphere to produce a mixture of stable fuels.
High yield of liquid range olefins obtained by converting i-propanol over zeolite H-ZSM-5
Mentzel, Uffe V.,Shunmugavel, Saravanamurugan,Hruby, Sarah L.,Christensen, Claus H.,Holm, Martin S.
experimental part, p. 17009 - 17013 (2010/03/23)
Methanol, ethanol, and i-propanol were converted under methanol-to-gasoline (MTH)-like conditions (400°C, 1-20 bar) over zeolite H-ZSM-5. For methanol and ethanol, the catalyst lifetimes and conversion capacities are comparable, but when i-propanol is use
