Preparation of high molecular weight, branched, acyclic polyalkyleneamines and mixtures thereof
US-9783486-B2 · Oct 10, 2017 · US
US9550725B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9550725-B2 |
| Application number | US-201214359134-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 19, 2012 |
| Priority date | Nov 25, 2011 |
| Publication date | Jan 24, 2017 |
| Grant date | Jan 24, 2017 |
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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.
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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.
Preparatory process · CPC title
by substitution of hydroxy groups or of etherified or esterified hydroxy groups · CPC title
Polyamines · CPC title
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