Process for preparation of di- and polyamines of the diphenylmethane series

Patent metadata

Field	Value
Publication number	US-10125091-B2
Application number	US-201515318102-A
Country	US
Kind code	B2
Filing date	Jun 22, 2015
Priority date	Jun 24, 2014
Publication date	Nov 13, 2018
Grant date	Nov 13, 2018

Abstract

The invention relates to a method for the preparation of di- and polyamines of the diphenylmethane series (MDA) from aniline and formaldehyde, care being taken during the start up that a sufficient excess of aniline with respect to formaldehyde is ensured, said excess amounting to at least 105% of the desired molar ratio of aniline to formaldehyde for the target recipe of the MDA to be produced.

First claim

The invention claimed is:

1. A process for preparing diamines and polyamines of the diphenylmethane series (MDA) by reaction of aniline (1) and formaldehyde (2) at a desired molar ratio of aniline (1) to formaldehyde (2) of A/F target , which comprises the steps:
either according to a variant A)
A.I) reacting aniline (1) and formaldehyde (2) in the absence of an acid catalyst (3) in a reactor to form an aminal, with aniline (1) and formaldehyde (2) being introduced into the reactor, and subsequent separation of the reaction mixture obtained into an aqueous phase and an organic, aminal-containing phase; and
A.II) reacting at least part of the organic, aminal-containing phase obtained in step A.I) with acid (3) in a reactor, with the aminal reacting to form diamines and polyamines of the diphenylmethane series;
wherein the following steps are carried out for start-up of the process and/or resumption of the process after an interruption of at least the step A.I):
A.I.1) introducing aniline (1) into the reactor of step A.I) at a mass flow rate m 1 commencing at the point in time to;
A.I.2) introducing of formaldehyde (2) into the reactor of step A.I), commencing at a point in time t 1 , starting from a mass flow rate m 2 =0 at the point in time t 1 to a mass flow rate m 2 =m 2,intended at the point in time t 2 , where t 2 >t 1 >t 0 ; and
A.II.1) in the case of interruption of the step A.II) too, introducing acid (3) into the reactor of step A.II) at the latest when, as soon as or after, organic, aminal-containing phase is introduced for the first time into the reactor of step A.II);
where the introduction of aniline (1) in step A.I.1) and the introduction of formaldehyde (2) in step A.I.2) occur in such a way that the instantaneous molar ratio of
the total aniline (1) introduced into the reactor of step A.I)
to
the total formaldehyde (2) introduced into the reactor of step A.I),
A/F inst , is always ≥2 and ≥1.05·A/F targets during the period of time from t 1 to t 2 ;

or according to a variant B),
B.I) reacting aniline (1) and acid (3) in a reactor to form a reaction mixture containing the anilinium salt of the acid (3) used; and
B.II) reacting of at least part of the reaction mixture obtained in step B.I) with formaldehyde (2) in a reactor, forming diamines and polyamines of the diphenylmethane series;
wherein the following steps are carried out for the start-up of the process and/or the resumption of the process after an interruption of the steps B.I) and B.II);
B.I.1) introducing aniline (1) into the reactor of step B.I) at an aniline mass flow rate m 1 commencing at the point in time t 0 ;
B.I.2) introducing of acid (3) before, simultaneously with or after introduction of aniline (1);
B.II.1) introducing of formaldehyde (2) into the reactor of step B.II), optionally together with further aniline (1), optionally together with further acid (3), commencing at a point in time t 1 , proceeding from a mass flow rate m 2 =0 at the point in time t 1 to a mass flow rate m 2 =m 2,intended at the point in time t 2 , where t 2 >t 1 >t 0 ;
where the introduction of aniline (1) in step B.I.1) and optionally in step B.II.1) and the introduction of formaldehyde (2) in step B.II.1) occur in such a way that the instantaneous molar ratio of
the total aniline (1) introduced into the reactor of step B.I) and, if present, the total aniline (1) introduced into the reactor of step B.II)
to
the total formaldehyde (2) introduced into the reactor of step B.II),
A/F inst , is always ≥2 and ≥1.05·A/F target during the period of time from t 1 to t 2 .

2. The process as claimed in claim 1 , wherein the steps I) and II) of both variants are carried out in a continuous process.

3. The process as claimed in claim 1 , wherein A/F target has a value of from 1.5 to 20 in both variants.

4. The process of claim 3 , wherein A/F target has a value of from 1.5 to 10 in both variants.

5. The process of claim 4 , wherein A/F target has a value of from 1.5 to 6 in both variants.

6. The process as claimed in claim 1 , wherein t 1 −t 0 is >0.001 hour in both variants.

7. The process as claimed in claim 1 wherein t 2 −t 1 is <30 hours in both variants.

8. The process as claimed in claim 1 , wherein the mass flow rate m 1 is ≥1000 kg/hour in both variants.

9. The process as claimed in claim 1 , wherein the mass flow rate m 2,intended is ≥300 kg/hour in both variants.

10. The process as claimed in claim 1 , wherein, in both variants, the point in time t 1 is selected so that at this point in time the respective reactor is full of aniline to an extent of from 1% to 99% of its maximum capacity.

11. The process of claim 10 , wherein, in both variants, the point in time t 1 is selected so that at this point in time the respective reactor is full of aniline to an extent of from 10% to 90% of its maximum capacity.

12. The process of claim 11 , wherein, in both variants, the point in time t 1 is selected so that at this point in time the respective reactor is full of aniline to an extent of from 20% to 80% of its maximum capacity.

Assignees

• Covestro Deutschland Ag

Inventors

• Knauf Thomas
• Wershofen Stefan
• Gruner Klaus-Gerd
• Hartjes Volker

Classifications

• C07C209/78 Primary

  from carbonyl compounds, e.g. from formaldehyde, and amines having amino groups bound to carbon atoms of six-membered aromatic rings, with formation of methylene-diarylamines · CPC title

• C07C211/50

  with at least two amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton · CPC title

• C07C211/49

  having at least two amino groups bound to the carbon skeleton · CPC title

• C07C209/82

  Purification; Separation; Stabilisation; Use of additives · CPC title

• B01J2219/0059

  Sequential processes · CPC title