Method for preparation of 1,4-cyclohexanedimethanol
US-11629112-B2 · Apr 18, 2023 · US
US2023192579A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2023192579-A1 |
| Application number | US-202218003432-A |
| Country | US |
| Kind code | A1 |
| Filing date | May 20, 2022 |
| Priority date | Jun 18, 2021 |
| Publication date | Jun 22, 2023 |
| Grant date | — |
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Provided are a tricyclodecane dimethanol composition, in which a ratio of structural isomers is controlled, and a preparation method thereof.
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What is claimed is: 1 . A tricyclodecane dimethanol composition, comprising 20 parts by weight to 35 parts by weight of a first structural isomer represented by the following Formula 1-1, 27 parts by weight to 42 parts by weight of a second structural isomer represented by the following Formula 1-2, and 27 parts by weight to 42 parts by weight of a third structural isomer represented by the following Formula 1-3: 2 . The tricyclodecane dimethanol composition of claim 1 , comprising 22 parts by weight to 30 parts by weight of the first structural isomer, 30 parts by weight to 36 parts by weight of the second structural isomer, and 32 parts by weight to 40 parts by weight of the third structural isomer, based on 100 parts by weight of the composition. 3 . A method of preparing a tricyclodecane dimethanol composition, the method comprising the steps of: performing a hydroformylation reaction by adding dropwise dicyclopentadiene while maintaining a mixed gas of hydrogen and carbon monoxide at a pressure 20 bar to 150 bar in the presence of a catalyst composition including a rhodium-containing catalyst compound and 5 moles to 200 moles of an organophosphorus compound per 1 mole of rhodium, and a dienophile; and performing a hydrogenation reaction of tricyclodecane dialdehyde obtained by the hydroformylation reaction in the presence of a hydrogenation catalyst, wherein the tricyclodecane dimethanol composition includes 20 parts by weight to 35 parts by weight of a first structural isomer represented by the following Formula 1-1, 27 parts by weight to 42 parts by weight of a second structural isomer represented by the following Formula 1-2, and 27 parts by weight to 42 parts by weight of a third structural isomer represented by the following Formula 1-3, based on 100 parts by weight of the composition: 4 . The method of claim 3 , wherein the organophosphorus compound is included in an amount of 10 moles to 100 moles per 1 mole of rhodium. 5 . The method of claim 3 , wherein in the hydroformylation reaction step, the dropwise addition of dicyclopentadiene is performed such that the number of moles of dicyclopentadiene added per minute with respect to 1 mmol of the rhodium element in the catalyst composition is 10 mmol to 10,000 mmol. 6 . The method of claim 3 , wherein the dienophile is one or more selected from the group consisting of maleic anhydride, tetracyanoethylene, maleic acid, maleonitrile, 2-methylenemalononitrile, dialkyl 2-methylenemalonate, 2-methylenemalonic acid, 2-methylenemalonaldehyde, 3-methylenepentane-2,4-dione, fumaraldehyde, ethene-1,1,2,2-tetracarbaldehyde, 1,4-benzoquinone, and dialkyl maleate. 7 . The method of claim 3 , wherein the dienophile is used in an amount of 0.001 part by weight to 1.0 part by weight, based on 100 parts by weight of the dicyclopentadiene. 8 . The method of claim 3 , wherein the hydroformylation reaction step is performed at 50° C. to 100° C. 9 . The method of claim 3 , wherein the hydrogenation catalyst is a Ru/C catalyst. 10 . The method of claim 3 , wherein the hydrogenation reaction is performed at a temperature of 80° C. to 250° C. and a pressure of 20 bar to 200 bar.
Acids or hydroxy compounds containing cycloaliphatic rings · CPC title
by oxo-reaction combined with reduction · CPC title
containing rhodium or compounds thereof · CPC title
Dicyclopentadienes; Hydrogenated dicyclopentadienes · CPC title
Carbon · CPC title
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