Processes for Producing Phenol
US-2015315111-A1 · Nov 5, 2015 · US
US2020055816A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2020055816-A1 |
| Application number | US-201916555710-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 29, 2019 |
| Priority date | Jan 30, 2015 |
| Publication date | Feb 20, 2020 |
| Grant date | — |
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 provides a method of making carboxylic acids from levulinic acid, such as succinic acid and 3-hydroxypropanoic acid, by reacting levulinic acid with an oxidant such as hydrogen peroxide under acidic or basic conditions.
Opening claim text (preview).
1 . A method of preparing a carboxylic acid, wherein the carboxylic acid is 3-hydroxypropanoic acid, comprising: forming a reaction mixture comprising levulinic acid, an oxidant, and a base, under conditions suitable to prepare the carboxylic acid. 2 . (canceled) 3 . The method of claim 1 , wherein the oxidant is hydrogen peroxide. 4 . The method of claim 3 , wherein the reaction mixture is substantially free of an oxidizing metal catalyst. 5 .- 12 . (canceled) 13 . The method of claim 1 , wherein the base is selected from the group consisting of sodium hydroxide and potassium hydroxide. 14 . The method of claim 1 , wherein the reaction mixture is at a temperature between about 75° C. and about 200° C. 15 . The method of claim 1 , wherein the method comprises: forming the reaction mixture comprising levulinic acid, hydrogen peroxide, and potassium hydroxide, wherein the reaction mixture is at a temperature between about 100° C. and about 150° C., thereby forming the 3-hydroxypropanoic acid. 16 . The method of claim 1 , wherein the reaction mixture is at a temperature between about 0° C. and about 50° C. such that the product of the forming step is 3-(hydroperoxy)propanoic acid, and the method further comprises: forming a second reaction mixture comprising the 3-(hydroperoxy)propanoic acid and a hydrogenation agent, under conditions suitable to form the 3-hydroxypropanoic acid. 17 . The method of claim 16 , wherein the hydrogenation agent is palladium on carbon. 18 . The method of claim 16 , wherein the method comprises: forming the reaction mixture comprising levulinic acid, hydrogen peroxide, and potassium hydroxide, wherein the reaction mixture is at about room temperature, thereby preparing 3-(hydroperoxy)propanoic acid; and forming the second reaction comprising the 3-(hydroperoxy)propanoic acid, hydrogen gas and palladium on carbon, under conditions suitable to form the 3-hydroxypropanoic acid. 19 . The method of claim 16 , further comprising prior to the second forming step: contacting the reaction mixture with an acid such that the pH of the reaction mixture is less than 7.0; and isolating the 3-(hydroperoxy)propanoic acid via extraction. 20 . The method of claim 19 , wherein the acid is selected from the group consisting of hydrofluoric acid, hydrochloric acid, hydrobromic acid, hypochloric acid, sulfuric acid, nitric acid, phosphoric acid, hexafluorophosphoric acid, methanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, trifluoromethanesulfonic acid, fluoroacetic acid, and trifluoroacetic acid. 21 . The method of claim 16 , wherein the method comprises: forming the reaction mixture comprising levulinic acid, hydrogen peroxide, and potassium hydroxide, wherein the reaction mixture is at about room temperature, thereby preparing 3-(hydroperoxy)propanoic acid; contacting the reaction mixture with hydrochloric acid such that the pH of the reaction mixture is less than 7.0; isolating the 3-(hydroperoxy)propanoic acid via extraction; and forming the second reaction comprising the 3-(hydroperoxy)propanoic acid, hydrogen and palladium on carbon, under conditions suitable to form the 3-hydroxypropanoic acid.
the carbon atom being acyclic · CPC title
Preparation of peroxy compounds · CPC title
by introduction of functional groups containing oxygen only in singly bound form · CPC title
with peroxy-compounds · CPC title
of peroxy of hydroperoxy groups · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.