Lipophilic polyalkylenepolyamines by homogeneously catalyzed alcohol amination

US9550725B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9550725-B2
Application numberUS-201214359134-A
CountryUS
Kind codeB2
Filing dateNov 19, 2012
Priority dateNov 25, 2011
Publication dateJan 24, 2017
Grant dateJan 24, 2017

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Process for the preparation of lipophilic polyalkylenepolyamines by homogeneously catalyzed alcohol amination, where aliphatic amino alcohols are reacted with one another or aliphatic diamines or polyamines are reacted with aliphatic diols or polyols with the elimination of water in the presence of a homogeneous catalyst, at least one of the reactants comprising an alkyl or alkylene group having five or more carbon atoms, and after the reaction a phase separation into at least one apolar phase and at least one polar phase being present, the lipophilic polyalkylenepolyamines being present in enriched form in the apolar phase. Polyalkylenepolyamines obtainable by such processes, and polyalkylenepolyamines comprising hydroxyl groups, secondary amines or tertiary amines. Uses of such polyalkylenepolyamines as adhesion promoters for printing inks, adhesion promoters in composite films, cohesion promoters for adhesives, crosslinkers/curing agents for resins, primers in paints, wet-adhesion promoters for emulsion paints, complexing agents and flocculating agents, penetration assistants in wood preservation, corrosion inhibitors, immobilizing agents for proteins and enzymes.

First claim

Opening claim text (preview).

The invention claimed is: 1. A process for preparing a lipophilic polyalkylenepolyamine, by homogeneously catalyzed alcohol amination, the process comprising: (i) reacting aliphatic amino alcohols with one another, or (ii) reacting an aliphatic diamine or polyamine with an aliphatic diol or polyol, to obtain a reaction mixture, with elimination of water, in the presence of a homogeneous transition metal complex catalyst, wherein: at least one starting material of the aliphatic amino alcohols, aliphatic diamine, polyamine, aliphatic diol or polyol comprises an alkyl or alkylene group having five or more carbon atoms; and the process further comprises, after the reacting, performing a phase separation into a nonpolar phase and a polar phase, such that the lipophilic polyalkylenepolyamine is present in enriched form in the nonpolar phase. 2. The process according to claim 1 , wherein at least one of the starting materials comprises an alkyl or alkylene group having from 5 to 50 carbon atoms. 3. The process according to claim 1 , wherein the catalyst is present in enriched form in the polar phase. 4. The process according to claim 1 , further comprising, after the reacting, adding a polar solvent to the reaction mixture. 5. The process according to claim 1 , wherein the catalyst comprises a nitrogen-heterocyclic carbene ligand. 6. The process according to claim 1 , wherein the catalyst comprises a monodentate or polydentate phosphine ligand. 7. The process according to claim 1 , wherein the catalyst comprises at least one ligand selected from the group consisting of cyclopentadienyl, a substituted cyclopentadienyl, indenyl and a substituted indenyl. 8. The process according to claim 1 , wherein the catalyst comprises at least one ligand selected from the group consisting of hydroxide, hydride, carbonyl and chloride. 9. The process according to claim 1 , wherein the reaction is carried out in the presence of a solvent or solvent mixture. 10. The process according to claim 1 , wherein heteroatoms O or N of one of the starting materials are located in alpha and beta position on a chain of carbon atoms and thus on adjacent carbon atoms. 11. The process according to claim 1 , wherein heteroatoms O or N of one of the starting materials are located in alpha and omega position on a chain of carbon atoms and thus at opposite ends of the chain of carbon atoms. 12. A polyalkylenepolyamine obtained by the process according to claim 1 , wherein a polydispersity of the polyalkylenepolyamine ranges from 2.4 to 37. 13. The polyalkylenepolyamine of claim 12 , comprising a hydroxyl group, secondary amine or tertiary amine. 14. A process for promoting adhesion, the process comprising adding the polyalkylenepolyamine according to claim 12 to an adhesive, wherein the polyalkylenepolyamine is an adhesion promoter for at least one selected from the group consisting of printing inks, composite films, and emulsion paints. 15. The process according to claim 1 , comprising (i) reacting the aliphatic amino alcohols with one another. 16. The process according to claim 1 , comprising (ii) reacting the aliphatic diamine or polyamine with the aliphatic diol or polyol. 17. The process according to claim 4 , wherein the catalyst comprises at least one ligand selected from the group consisting of hydroxide, hydride, carbonyl and chloride.

Assignees

Inventors

Classifications

  • Preparatory process · CPC title

  • C07C209/14Primary

    by substitution of hydroxy groups or of etherified or esterified hydroxy groups · CPC title

  • Polyamines · CPC title

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What does patent US9550725B2 cover?
Process for the preparation of lipophilic polyalkylenepolyamines by homogeneously catalyzed alcohol amination, where aliphatic amino alcohols are reacted with one another or aliphatic diamines or polyamines are reacted with aliphatic diols or polyols with the elimination of water in the presence of a homogeneous catalyst, at least one of the reactants comprising an alkyl or alkylene group havin…
Who is the assignee on this patent?
Basf Se
What technology area does this patent fall under?
Primary CPC classification C08G73/0213. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).