Reductive preparation of tertiary dimethylamines from nitriles
US-2016368856-A1 · Dec 22, 2016 · US
US10906865B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10906865-B2 |
| Application number | US-201716337262-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 28, 2017 |
| Priority date | Oct 4, 2016 |
| Publication date | Feb 2, 2021 |
| Grant date | Feb 2, 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.
A method for producing 1,4-dicyanocyclohexane, having a step of obtaining 1,4-dicyanocyclohexane by subjecting a heated concentrate of an aqueous ammonia solution of 1,4-cyclohexanedicarboxylic acid to a cyanation reaction.
Opening claim text (preview).
The invention claimed is: 1. A method for producing 1,4-dicyanocyclohexane, comprising: obtaining 1,4-dicyanocyclohexane by subjecting a heated concentrate of an aqueous ammonia solution of 1,4-cyclohexanedicarboxylic acid to a cyanation reaction. 2. The method according to claim 1 , further comprising: obtaining the 1,4-cyclohexanedicarboxylic acid by subjecting terephthalic acid in an aqueous ammonia solution to a hydrogenation reaction. 3. The method according to claim 2 , wherein at least a part of an aqueous ammonia solution included in a reaction solution after obtaining 1,4-cyclohexanedicarboxylic acid is used as the aqueous ammonia solution in the obtaining of 1,4-dicyanocyclohexane. 4. The method according to claim 2 , wherein the reaction solution after the obtaining of 1,4-cyclohexanedicarboxylic acid is used as a raw material solution for the obtaining of 1,4-dicyanocyclohexane, without collecting 1,4-cyclohexanedicarboxylic acid by filtration therefrom. 5. The method according to claim 1 , further comprising obtaining the heated concentrate by heating the aqueous ammonia solution of 1,4-cyclohexanedicarboxylic acid to 100 to 200° C. to remove at least a part of water. 6. The method according to claim 3 , wherein the reaction solution after obtaining 1,4-cyclohexanedicarboxylic acid is used as a raw material solution for the obtaining of 1,4-dicyanocyclohexane, without collecting 1,4-cyclohexanedicarboxylic acid by filtration therefrom. 7. The method according to claim 2 , further comprising obtaining the heated concentrate by heating the aqueous ammonia solution of 1,4-cyclohexanedicarboxylic acid to 100 to 200° C. to remove at least a part of water. 8. The method according to claim 3 , further comprising obtaining the heated concentrate by heating the aqueous ammonia solution of 1,4-cyclohexanedicarboxylic acid to 100 to 200° C. to remove at least a part of water. 9. The method according to claim 4 , further comprising obtaining the heated concentrate by heating the aqueous ammonia solution of 1,4-cyclohexanedicarboxylic acid to 100 to 200° C. to remove at least a part of water. 10. The method according to claim 6 , further comprising obtaining the heated concentrate by heating the aqueous ammonia solution of 1,4-cyclohexanedicarboxylic acid to 100 to 200° C. to remove at least a part of water.
by reduction of nitriles · CPC title
The ring being saturated · CPC title
containing at least two amino groups bound to the carbon skeleton · CPC title
Completely hydrogenated benzenedicarboxylic acids · CPC title
by reaction of ammonia with carboxylic acids with replacement of carboxyl groups by cyano groups · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.