Process for reductively aminating ketones and aldehydes with aqueous amines and catalysts suitable therefor
View Patent ↗A process for preparing amines of the general formula (I) R 1 R 2 CHNR 3 R 4 (I) in which R 1 , R 2 , R 3 and R 4 are each independently hydrogen, straight-chain or branched, halogenated or halogen-free C 1 -C 12 -alkyl, C 3 -C 12 -cycloalkyl, C 6 -C 10 -aryl or C 7 -C 11 -aralkyl, by catalytic, hydrogenating amination of carbonyl compounds of the general formula (II) R 1 —C(═O)—R 2 (II) with nitrogen compounds of the general formula (III) HNR 3 R 4 (III) in the presence of bifunctional catalyst systems comprising a.) a hydrogenation-active catalyst component comprising one or more metals of transition group 8 of the Periodic Table and b.) one or more solid, acidic cocatalysts, wherein the hydrogenating amination is carried out in the presence of aqueous ammonia or aqueous amine of the formula (III) and at least one organic solvent miscible with ammonia or the aqueous amine of the formula (III).
1. A process for preparing amines of the general formula (I)
R 1 R 2 CHNR 3 R 4 (I)
in which R 1 , R 2 , R 3 and R 4 are each independently hydrogen, straight-chain or branched, halogenated or halogen-free C 1 -C 12 -alkyl, C 3 -C 12 -cycloalkyl, C 6 -C 10 -aryl or C 7 -C 11 -aralkyl, said process comprising catalytic, hydrogenating amination of a carbonyl compound of the general formula (II)
R 1 —C(═O)—R 2 (II)
with a nitrogen compound of the general formula (III)
HNR 3 R 4 (III)
in the presence of a bifunctional catalyst comprising a.) a hydrogenation-active catalyst component comprising a metal selected from the group consisting of Pt, Pd and mixtures thereof disposed on carbon and b.) one or more solid, acidic cocatalysts selected from the group consisting of Al 2 O 3 , TiO 2 , SiO 2 , ZrO 2 , and mixtures thereof, wherein the hydrogenating amination is carried out in a reaction mixture in the presence of an aqueous solution being an aqueous ammonia or aqueous amine of the formula (III) and at least one organic solvent miscible with ammonia or the aqueous amine of the formula (III).
2. The process as claimed in claim 1 , wherein the aqueous solution has an amine concentration in the range from 0.1 to 80% by weight.
3. The process of claim 1 , wherein the one or more solid acidic cocatalysts provides support for the second hydrogenation-active catalyst component.
4. The process of claim 1 , wherein the hydrogenation-active catalyst component and the one or more solid acidic cocatalysts are present in suspension.
5. The process of claim 1 , wherein the carbonyl compound is selected from the group consisting of methylacetophenone, fluoroacetophenone, benzaldehyde, fluorobenzaldehyde, and 4,4′-dichlorobenzophenone.
6. The process of claim 1 , wherein the nitrogen compound is selected from the group consisting of methylamine, ethylamine, propylamine, dimethylamine, diethylamine, dipropylamine, ammonia, and mixtures thereof.
7. The process of claim 1 , wherein the at least one organic solvent is present in the reaction mixture in the, range from 20 to 85% by weight.
8. The process of claim 1 , wherein the organic solvent miscible with amine is at least one polar protic solvent.
9. The process of claim 1 , wherein the at least one solid acidic cocatalyst is selected from the group consisting of TiO 2 , ZrO 2 , and mixtures thereof.
10. The process of claim 8 , wherein the at least one polar protic solvent is an alcohol or water or a mixture thereof.
11. The process of claim 6 , wherein the nitrogen compound is ammonia.
12. The process of claim 1 , wherein the hydrogenating amination is carried out in the presence of aqueous amine solution having a concentration in the range from 1 to 25% by weight.