Preparation of diamine via the preparation of aminonitrile
View Patent ↗A continuous method (P) for preparing diamine is described. The method includes reacting the corresponding alkene nitrile with the corresponding monoamine in order to form the corresponding aminonitrile. The monoamine can be introduced in molecular excess with respect to the alkene nitrile, wherein the unreacted monoamine is recirculated to the reaction; followed by reducing the aminonitrile produced by hydrogen in the presence of at least one alkali-metal hydroxide, water, and a hydrogenation catalyst; and purifying the diamine.
1. A continuous process (P) for continuously preparing a diamine, the process comprising the steps of:
(a) reacting a corresponding alkenenitrile and a corresponding monoamine to form a corresponding aminonitrile, the monoamine being introduced in molar excess relative to the alkenenitrile, with recycling into the reaction of the unreacted monoamine;
(b) reducing the aminonitrile obtained in step (a) with hydrogen in the presence of at least one alkali metal hydroxide, water and a hydrogenation catalyst;
(c) separating the at least one alkali metal hydroxide by evaporation of a diamine obtained in step (b) and of the water; and
(d) distilling the diamine,
wherein, said alkenenitrile is a linear or branched C2 to C4 alkene in which a hydrogen atom is replaced with a conjugated cyano group and/or the monoamine is a secondary amine of general formula R1R2NH, in which R1 and R2, which can be identical or different, represent a C1 to C4 alkyl.
2. The process as claimed in claim 1 , wherein the monoamine is dimethylamine, the alkenenitrile is acrylonitrile, the aminonitrile is 3-(dimethylamino)propanenitrile and the diamine is dimethylaminopropylamine.
3. The process as claimed in claim 1 , wherein step (a) is performed in one or more reactors in series of piston type with recycling of the excess monoamine and recycling of some of the aminonitrile.
4. The process as claimed in claim 1 , wherein in step (a), the monoamine is introduced in an excess of at least 0.1 mol % relative to the alkenenitrile.
5. The process as claimed in claim 1 , wherein the recycling of the monoamine uses a separation system, which makes it possible to recover:
the aminonitrile, a first fraction of which is sent to a reactor for step (b) and a second fraction of which is sent to an absorption system to enable dissolution of the excess monoamine; and
the excess monoamine in gaseous form, which is sent to said absorption system which enables its dissolution in said second fraction of aminonitrile.
6. The process as claimed in claim 1 , wherein step (b) is performed in a reactor comprising means for separating out catalyst.
7. The process as claimed in claim 1 , wherein the catalyst of step (b) is separated out, and all or part of this catalyst is regenerated before being recycled into the reaction (b).
8. The process as claimed in claim 1 , wherein the catalyst of step (b) is a Raney metal.
9. The process as claimed in claim 1 , wherein a fraction of alkali metal hydroxide that is soluble in the reaction medium is removed by means of an evaporator; and
the water and the majority of the diamine derived from step (b) pass into vapor phase and are directed toward a distillation column for step (d).
10. The process as claimed in claim 9 , for which a residual fraction of diamine associated with the alkali metal hydroxide leaving the evaporator is recovered by decantation after dissolution of the alkali metal hydroxide in water.
11. The process as claimed in claim 1 , wherein in step (c), the distillation is performed using a side-withdrawal column or a wall column.
12. The process as claimed in claim 5 , wherein the separation system is a flash column and/or a distillation column.
13. The process as claimed in claim 6 , wherein the means for separating out the catalyst is a decanter and/or a tangential filtration system.
14. The process as claimed in claim 8 , wherein the Raney metal is doped Raney nickel.