IP Library Granted Patent US 7,586,004
Granted Patent B2
US 7,586,004 · App. 10/556,798 · Granted Sep 8, 2009

Method for continuously producing alkylamino(meth)acrylamides

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Quick Facts
Patent No.
US 7,586,004
App. No.
10/556,798
Granted
Sep 8, 2009
Kind
B2
Abstract

The invention relates to a process for continuously preparing alkylamino(meth)acrylamide by reacting methyl (meth)acrylate, ethyl (meth)acrylate or amines having a high boiling point compared to methanol or ethanol. A special workup technique which includes removing water from the amine before entering the reactor allows product qualities which have hitherto not been attained to be achieved. In addition, very high space-time and overall yields can be achieved.

Claims (59)

1. A continuous process of high catalyst efficiency and product purity for the preparation of an alkylamino(meth)acrylamide of formula (C) in a suitable reaction apparatus,

where R 1 is an H or CH 3 group and R 2 is a linear, branched or cyclic alkyl radical or aryl radical having 2 to 12 carbon atoms,

the process comprising:

continuously feeding to the suitable reaction apparatus:

an amine of formula (B):

R 2 NH 2   (B)

a compound of formula (A):

wherein R 3 is methyl or ethyl,

a transesterification catalyst, and

at least one polymerization inhibitor;

removing water from the amine of formula (B);

reacting the amine of formula (B) from which the water was removed, with the compound of formula (A) to form a reaction mixture comprising the alkylamino(meth)acrylamide of formula (C);

continuously removing an azeotropic mixture comprising an alcohol of formula (D):

R 3 OH  (D)

and the compound of formula (A) to an azeotropic distillation column;

continuously conducting the reaction mixture out of the at least one reactor to a gentle film evaporator; and

purifying a bottom stream from the gentle film evaporator in a purifying distillation column;

wherein

in the continuous feeding, the amine of formula (B) is fed to the at least one reactor via the azeotropic distillation column, and

the suitable reaction apparatus comprises:

at least one reactor,

an azeotropic distillation column connected to the at least one reactor,

a gentle film evaporator connected to the at least one reactor,

a low boiler distillation column connected to the falling film evaporator at a lower position of the low boiler distillation column and connected to the azeotropic distillation column at an upper position of the low boiler distillation column, and

a purifying distillation column connected to the falling film evaporator.

2. The process according to claim 1 , wherein

a stream of the gentle film evaporator is fed continuously to a purifying distillation column in which the highly pure product amide of the formula (C) is removed via the top by distillation under reduced pressure, and the catalyst and the polymerization inhibitors, and also the high-boiling by-products with a small portion of product amide of the formula (C) are removed via the bottom.

3. The process according to claim 1 , wherein

the amine of formula (B) is dewatered in the azeotropic distillation column connected to the at least one reactor.

4. The process according to claim 1 , wherein

a molar ratio of the compound of formula (A) to the amine of formula (B) in the feed to the reactor is between 1 and 2.

5. The process according to claim 1 , wherein

the transesterification catalyst is a tetraalkyl titanate.

6. The process according to claim 1 , wherein

an amount of transesterification catalyst is 0.1-10% by weight, based on an amount of the compound of formula (A).

7. The process according to claim 6 , wherein

the amount of transesterification catalyst is 0.2-7% by weight.

8. The process according to claim 1 , wherein

the transesterification catalyst is a mixture of dioctyltin oxide and isopropyl titanate in a ratio of 1:1 in % by weight.

9. The process according to claim 8 , wherein

an amount of the transesterification catalyst mixture is 0.1-10% by weight, based on the amount of the compound of formula (A).

10. The process according to claim 2 , wherein

the amount of the transesterification catalyst mixture is 0.2-7% by weight.

11. The process according to claim 1 , wherein

the polymerization inhibitor is at least one selected from the group consisting of phenothiazine, tert-butylcatechol, hydroquinone monomethyl ether, hydroquinone and mixtures thereof, and an amount of the polymerization inhibitor is between 100 and 5000 ppm, based on the weight of the reaction mixture.

12. The process according to claim 1 , wherein

the polymerization inhibitor comprises oxygen.

13. The process according to claim 1 , wherein

the amine of formula (B) is dimethylaminopropylamine.

14. The process according to claim 1 , wherein

a pressure in the low boiler distillation column is between 20 and 500 mbar.

15. The process according to claim 1 , wherein

a residence time of the reaction mixture in the suitable reaction apparatus is between 0.5 and 1.5 hours.

16. The process according to claim 4 ,

wherein

the molar ratio of the compound of formula (A) to the amine of formula (B) in the feed to the reactor is in the range from 1.05 to 1.15.

17. The process according to claim 2 , wherein a pressure within the purifying distillation column is in the range from 20 to 200 mbar.

18. The process according to claim 2 , wherein the gentle film evaporator is an evaporator selected from the group consisting of a falling film evaporator, a thin-layer evaporator and a short-path evaporator.

19. The process according to claim 18 , wherein the gentle film evaporator is a falling film evaporator.

Assignments (11)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 20, 2020
From: RÖHM GMBH
To: EVONIK OIL ADDITIVES GMBH
Reel/Frame 052194/0550 →
CHANGE OF NAME Recorded Mar 20, 2020
From: EVONIK RÖHM GMBH
To: RÖHM GMBH
Reel/Frame 052194/0462 →
MERGER Recorded Mar 20, 2020
From: EVONIK OIL ADDITIVES GMBH
To: EVONIK DEGUSSA GMBH
Reel/Frame 052195/0001 →
CHANGE OF NAME Recorded Mar 20, 2020
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 052195/0226 →
CHANGE OF NAME Recorded Feb 25, 2010
From: ROHM GMBH
To: EVONIK ROHM GMBH
Reel/Frame 023998/0789 →
CHANGE OF ENTITY Recorded Feb 25, 2010
From: ROHM GMBH & CO. KG
To: ROHM GMBH
Reel/Frame 023998/0760 →
CHANGE IN LEGAL FORM Recorded Nov 18, 2009
From: ROEHM GMBH & CO. KG
To: ROEHM GMBH
Reel/Frame 023536/0346 →
CHANGE OF NAME Recorded Nov 18, 2009
From: ROEHM GMBH
To: EVONIK ROEHM GMBH
Reel/Frame 023536/0485 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S NAME PREVIOUSLY RECORDED ON REEL 018941 FRAME 0063. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 2, 2007
From: SCHLEEP, VOLKER; MERTZ, THOMAS
To: ROEHM GMBH & CO. KG
Reel/Frame 018955/0361 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S NAME PREVIOUSLY RECORDED ON REEL 018863 FRAME 0523. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Feb 28, 2007
From: SCHLEEP, VOLKER; MERTZ, THOMAS
To: ROEHM GMBH CO. KG
Reel/Frame 018941/0063 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2007
From: SCHLEEP, VOLKER; MERTZ, THOMAS
To: ROEHM GMBH
Reel/Frame 018863/0523 →