Polyethers, polyamines, polythioethers, and methods for making same
US-2017283553-A1 · Oct 5, 2017 · US
US11008271B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11008271-B2 |
| Application number | US-201716331889-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 8, 2017 |
| Priority date | Sep 8, 2016 |
| Publication date | May 18, 2021 |
| Grant date | May 18, 2021 |
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 invention is directed to methods of producing alkoxylated or hydroxylated terpenes comprising the steps of continuously passing a solution comprising an alcohol in combination with a terpene over an acidic resin catalyst in a packed bed reactor in order to yield a product, as well as compounds that are the products of the methods described herein.
Opening claim text (preview).
The invention claimed is: 1. A method of producing an alkoxylated terpene comprising the step of: continuously passing a solution comprising methanol, in combination with the terpene over an acidic resin catalyst in a packed bed reactor in order to yield a product, wherein the acidic resin catalyst is selected from a propanesulfonic acid resin, or a montmorillonite, or a macroreticular or cellular resin covalently bonded to sulfonic acid or carboxylic acid groups, or a silica covalently bonded to sulfonic acid or carboxylic acid groups, and wherein said terpene is valencene. 2. The method of claim 1 , wherein the average residence time for said solution in the packed bed reactor is between 0 minutes and 30 minutes. 3. The method of claim 1 , wherein said acidic resin catalyst is packed into a tube or a pipe through which said solution flows. 4. The method of claim 1 , wherein products are purified through distillation. 5. A compound of Formula (II) described by the following structure: 6. A fragrance composition, perfume composition, soap composition, flavor composition, or flavorant composition, comprising a compound according to claim 5 . 7. The method of claim 1 , wherein the acidic resin catalyst is a silica covalently bonded to sulfonic acid or carboxylic acid groups. 8. The composition according to claim 6 , wherein the composition is a fragrance composition. 9. The composition according to claim 6 , wherein the composition is a perfume composition. 10. The composition according to claim 6 , wherein the composition is a soap composition. 11. The composition according to claim 6 , wherein the composition is a flavor composition. 12. The composition according to claim 6 , wherein the composition is a flavorant composition.
containing three- or four-membered rings · CPC title
containing rings other than six-membered aromatic rings · CPC title
by hydration of carbon-to-carbon double bonds · CPC title
by addition of organic compounds only · CPC title
both rings being six-membered · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.