A method for synthesizing xanthohumol
US-2024239732-A1 · Jul 18, 2024 · US
US9018408B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9018408-B2 |
| Application number | US-201213977935-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 10, 2012 |
| Priority date | Mar 14, 2011 |
| Publication date | Apr 28, 2015 |
| Grant date | Apr 28, 2015 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention generally relates to a condensed process for producing terephthalic acid and terephthalic esters from a dialkyl cyclohexane-2,5-dione-1,4-dicarboxylate; a chemoselective process for preparing a substantially bicyclic-lactone-free dialkyl cyclohexane-2,5-diol-1,4-dicarboxylate; and compositions of matter prepared thereby.
Opening claim text (preview).
What is claimed is: 1. A condensed process for preparing a dialkyl terephthalate, the condensed process comprising a one-pot portion comprising steps (a) to (c): (a) contacting a mixture comprising dialkyl cyclohexane-2,5-dione-1,4-dicarboxylate and an oxygen-containing solvent with hydrogen (H2) gas and a hydrogenating effective amount of a dual-function supported metal catalyst under hydrogenating effective conditions to give a dialkyl cyclohexane-2,5-diol-1,4-dicarboxylate, wherein the dual-function supported metal catalyst comprises a metal that can facilitate reduction and dehydrogenation and the metal is deposited on a solid support; (b) contacting the dialkyl cyclohexane-2,5-diol-1,4-dicarboxylate with a dehydrating effective amount of a dehydration catalyst under dehydrating effective conditions to give dialkyl dihydrobenzene-1,4-dicarboxylate; and (c) the dialkyl dihydrobenzene-1,4-dicarboxylate is dehydrogenated via the dual-function supported metal catalyst from step (a); wherein steps (a) to (c) are performed in a same reactor and the oxygen-containing solvent of step (a) is carried through and also employed in steps (b) and (c). 2. The condensed process as in claim 1 , wherein the dialkyl cyclohexane-2,5-diol-1,4-dicarboxylate has less than 5 weight percent of a bicyclic lactone by-product. 3. The process as in claim 1 , wherein the metal of the dual-function supported metal catalyst is Ir, Ni, Ru, Rh, Pd, Pt, or a combination thereof.
by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups · CPC title
Terephthalic acid esters · CPC title
by elimination of functional groups containing oxygen only in singly bound form · CPC title
by introduction of functional groups containing oxygen only in singly bound form · CPC title
by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.