Process for obtaining amines by reduction of amides
View Patent ↗Disclosed is a process for the preparation of primary, secondary and tertiary amines via a catalytic hydrogenation of unsubstituted, N-substituted, and N,N-disubstituted amides. The amide is led, together with an auxiliary amine, in vaporised form in a hydrogen containing gas flow over the catalyst. The process can be carried out at relatively low pressures, between 2 and 50 bars, using typical hydrogenation catalysts like CuCr-type catalysts. The amine is obtained with high yield and high selectivity. The process can be carried out in a continuous fixed bed reactor.
1. A process for preparing an amine with following formula:
comprising the reduction of an amide of following formula:
with H 2 in the presence of an auxiliary amine of the following formula:
wherein said H 2 , said auxiliary amine and said amide are all led completely in a gaseous form, in a gaseous stream, over a hydrogenation catalyst, at a reaction pressure higher than 2 but lower than 50 bars, and wherein:
R1 is H or a saturated or unsaturated hydrocarbon group containing from 1 to 23 carbon atoms;
R2 and R3 are independently H or a hydrocarbon group containing from 1 to 8 carbon atoms, and
R4 is equal to R1 but may show a different degree of unsaturation.
2. A process according to claim 1 , wherein said reduction reaction is performed under a reaction pressure higher than or equal to 3 bars.
3. A process according to claim 1 , characterised in that said reduction reaction is performed under a reaction pressure lower than 45 bars.
4. A process according to claim 1 , characterised in that said gaseous stream is composed to contain, per mole of said amide, at least N c moles of carrier gasses which comprise at least said auxiliary amine and said H 2 ; with
N
c
=
P
tot
-
VP
a
VP
a
wherein: P tot =the reaction pressure; and
VP a =the saturated vapour pressure of the amide at the reaction temperature.
5. A process according to claim 1 , wherein the auxiliary amine is added in an amount of 0.05 to 40 moles per mole of said amide.
6. A process according to claim 1 , wherein R2 and R3 are the same and consist of a hydrocarbon group with 1 to 4 carbon atoms and wherein said reduction is carried out in the presence of said auxiliary amine and in the presence of a further auxiliary amine with following formula:
(R2) 3 N.
7. A process according to claim 1 , wherein after having led the amide and the auxiliary amine in said gaseous stream over the catalyst, a product containing the amine which is to be prepared is separated off from the gaseous stream.
8. A process according to claim 7 , wherein the hydrogen and the auxiliary amine are led together with said amide in such an amount over the hydrogenation catalyst that said product contains less than 2 parts by weight of R1CH 2 OH per 100 parts by weight of the sum of said amine, said amide, R1CH 2 OH, (R1CH 2 ) 2 NR2 and (R1CH 2 ) 2 NR3.
9. A process according to claim 7 , wherein the hydrogen and the auxiliary amine are led together with said amide in such an amount over the hydrogenation catalyst that said product contains less than 5 parts by weight of the sum of (R1CH 2 ) 2 NR2 and (R1CH 2 ) 2 NR3 per 100 parts by weight of the sum of said amine, said amide, R1CH 2 OH, (R1CH 2 ) 2 NR2 and (R1CH 2 ) 2 NR3.
10. A process according to claim 7 , wherein after having separated the amine which is to be prepared off from the gaseous stream, at least a portion of the hydrogen and of the auxiliary amine which are still present is the gaseous stream are recycled to the catalyst.
11. A process according to claim 7 , wherein the amine which is to be prepared is a tertiary amine with R2 and R3 being the same and wherein said product is subjected to an alkylation reaction to convert any secondary amine present therein into said tertiary amine.
12. A process according to claim 1 , wherein said amide is led over the catalyst with a sufficient contact time to convert more than 95wt % of the said amide.
13. A process according to claim 1 , wherein said catalyst is a fixed bed catalyst.
14. A process according to claim 1 , wherein R2 and R3 are a hydrocarbon group containing from 1 to 8 carbon atoms.
15. A process according to claim 14 , wherein R2 and R3 are a hydrocarbon group containing from 1 to 4 carbon atoms.
16. A process according to claim 1 , wherein R1 is a saturated or unsaturated hydrocarbon group containing at least 1 carbon atom.
17. A process according to claim 1 , wherein R 1 is a saturated or unsaturated hydrocarbon group containing at the most 20 carbon atoms.
18. A process according to claim 1 , wherein said amine, including any secondary amine when said amine is a tertiary amine wherein R2 and R3 are the same, is produced in greater than 90% selectivity.
19. A process according to claim 1 , wherein said H 2 , said auxiliary amine and said amide are led at a temperature of between 100 and 310° C. over the hydrogenation catalyst.
20. A process according to claim 19 , wherein said temperature is comprised between 100 and 290° C.
21. A process according to claim 16 , wherein R1 is a saturated or unsaturated hydrocarbon group containing at least 3 carbon atoms.
22. A process according to claim 21 , wherein R1 is a saturated or unsaturated hydrocarbon group containing at least 5 carbon atoms.
23. A process according to claim 22 , wherein R1 is a saturated or unsaturated hydrocarbon group containing at least 7 carbon atoms.