IP Library › Granted Patent US 12,091,480
Granted Patent B2
US 12,091,480 · App. 17/041,746 · Granted Sep 17, 2024

Method for producing 2-dimethylaminoethyl (meth)acrylate

Inventors: Cédrick Favero (Andrezieux Boutheon, FR); Johann Kieffer (Andrezieux Boutheon, FR); Jing Ling (Taixing, CN)
Assignee: SNF GROUP
C08F220/34C07C213/08C07C213/10C07C219/08
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Quick Facts
Patent No.
US 12,091,480
App. No.
17/041,746
Granted
Sep 17, 2024
Kind
B2
Abstract

Process for the production of 2-dimethylaminoethyl (meth)acrylate in multiple stage batch reactions involving the recycling of the catalyst (DBTO) in subsequent reaction, the addition a certain amount of fresh catalyst to the recycled catalyst, the use of said catalysts in the subsequent reaction, and wherein the volume decrease due to azeotropic distillation is compensate in order to keep the volume constant in the reactor during the reaction by the continuous addition of a composition comprising methyl(meth)acrylate and dimethylaminoethanol.

Claims (42)

1. A process for the production of 2-dimethylaminoethyl (meth)acrylate comprising a total of at least two and up to twenty sequential batch reactions wherein in each batch reaction, methyl(meth)acrylate, dimethylaminoethanol, dibutyltin oxide as catalyst, and a solvent are added as initial charge in an agitated reactor equipped with a distillation column, wherein an azeotropic distillation is made continuously during the reaction, wherein the volume decrease due to said azeotropic distillation is compensated in order to keep the volume constant in the reactor during the reaction by the continuous addition of a composition comprising methyl(meth)acrylate and dimethylaminoethanol, said composition may also comprise dibutyltin oxide said process comprising:

a first batch reaction wherein the dibutyltin oxide used as catalyst is a fresh dibutyltin oxide;

a separation step wherein the dibutyltin oxide from the first batch reaction is recovered from the reaction mixture of the first batch reaction, and that constitutes a recycled dibutyltin oxide;

at least a second batch reaction wherein at least 65% by weight of the recycled dibutyltin oxide is used with fresh dibutyltin oxide as catalyst of the second batch reaction:

wherein the amount of fresh dibutyltin oxide is comprised between 0.1% by weight and 35% by weight based on the recycled dibutyltin oxide from the first batch reaction,

wherein the mass proportion of recycled dibutyltin oxide and fresh dibutyltin oxide, added in the initial charge is comprised between 220/1 and 80/20, and

wherein the mass proportion of recycled dibutyltin oxide and fresh dibutyltin oxide is between 100/0 and 0/100, in the composition continuously added to compensate the azeotropic distillation, when said composition comprises dibutyltin oxide;

wherein in each batch reaction, the recycled dibutyltin oxide from the previous reaction is used in combination with fresh dibutyltin oxide as catalyst, and

wherein the solvent is an alkane from C6 to C12, linear, cyclic or branched.

2. The process according to claim 1 wherein the process comprises at least one subsequent batch reaction wherein at least 65% by weight of the recycled dibutyltin oxide from the previous reaction is used with fresh dibutyltin oxide as catalyst of said reaction:

wherein the amount of fresh dibutyltin oxide is comprised between 0.1% by weight and 35% by weight based on the recycled dibutyltin oxide from the previous reaction,

wherein the mass proportion of recycled dibutyltin oxide from the previous reaction and fresh dibutyltin oxide, added in the initial charge is comprised between 220/1 and 80/20, and

wherein the mass proportion of recycled dibutyltin oxide from the previous reaction and fresh dibutyltin oxide is between 100/0 and 0/100, in the composition continuously added to compensate the azeotropic distillation, when said composition comprises dibutyltin oxide.

3. The process according to claim 1 , wherein the sequential batch reactions of the process are made in the same reactor.

4. The process according to claim 1 , wherein the composition comprising methyl(meth)acrylate and dimethylaminoethanol that is continuously added during the reaction to compensate the volume decrease due to the azeotropic distillation comprises methyl(meth)acrylate, dimethylaminoethanol, dibutyltin oxide and solvent.

5. The process according to claim 1 , wherein the composition comprising methyl(meth)acrylate and dimethylaminoethanol that is continuously added during the reaction to compensate the volume decrease due to the azeotropic distillation is the same as the composition initially added in the reactor before the beginning of the reaction.

6. The process according to claim 1 , wherein in the second and/or in the subsequent batch reaction, at least 80% by weight of the recycled dibutyltin oxide recovered from the previous reaction is used with fresh dibutyltin oxide as catalyst of the subsequent reaction.

7. The process according to claim 1 , wherein the amount of fresh dibutyltin oxide in each of the subsequent reactions is between 0.1% by weight and 20% by weight based on the recycled dibutyltin oxide.

8. The process according to claim 1 , wherein in each subsequent batch reaction, the mass ratio of recycled dibutyltin oxide and fresh dibutyltin oxide, added in the initial charge of each of the subsequent reaction is between 97/3 and 85/15.

9. The process according to claim 1 , wherein the mass ratio of recycled dibutyltin oxide and fresh dibutyltin oxide, in the composition continuously added to compensate the azeotropic distillation in order to keep the volume constant in the reactor in case of comprising dibutyltin oxide, is between 95/5 and 5/95.

10. A process for the production of a polymer of 2-dimethylaminoethyl (meth)acrylate, comprising:

performing the process according to claim 1 , thereby producing 2-dimethylaminoethyl (meth)acrylate; and

polymerizing said 2-dimethylaminoethyl (meth)acrylate to obtain the polymer.

11. The process according to claim 1 , further comprising performing a separation step to recover a 2-dimethylaminoethyl (meth)acrylate mixture from reaction mixture obtained according to the process of claim 1 .

12. The process according to claim 1 , wherein the process produces a quaternized version of 2-dimethylaminoethyl (meth)acrylate or a quaternized version of a 2-dimethylaminoethyl (meth)acrylate mixture.

13. The process according to claim 10 , wherein the polymer is made with a quaternized version of 2-dimethylaminoethyl (meth)acrylate.

14. The process according to claim 10 , wherein the polymer is obtained by the polymerization of a quaternized version of 2-dimethylaminoethyl (meth)acrylate and at least one monomer selected from the following list:

non-ionic monomers: acrylamide, methacrylamide, N,N-dimethylacrylamide, N,N-diethylacrylamide, N-vinylpyrrolidone, N-vinylformamide, N-vinyl imidazole, the methacrylates of polyethylene glycol, diacetoneacrylamide, N-isopropylacrylamide, 2-hydroxyethyl acrylate, 2,3-dihydroxypropyl acrylate, 2-hydroxyethyl methacrylate, 2,3-dihydroxypropyl methacrylate, N-tert-butylacrylamide,

anionic monomers: acrylic acid, 2-acrylamido-2-methylpropane sulfonic acid (ATBS), methacrylic acid, itaconic acid, maleic acid, ally sulfonate, non-salified, partially or completely salified,

cationic monomers: diallyldimethylammonium chloride (DADMAC), acrylamido dialkylaminopropyl, methacrylamido dialkylaminopropyl, and their acidified or quaternized salts,

structure agent: polyethylenically unsaturated monomers having at least two unsaturated functional groups, selected from the group consisting of: vinyl, allyl, acrylic, epoxy functional groups, methylenebisacrylamide (MBA), triallylamine, tetrallylammonium chloride; or by macroinitiators such as the polyperoxides, polyazo compounds and transfer polyagents such as polymercaptan polymers.

15. The process according to claim 10 , further comprising adding the polymer to an aqueous solution in a method for water treatment, sludge dewatering, papermaking process, agriculture, cosmetic and detergency composition, textile process, oil and gas recovery process, fracturing, or mining operation.

16. The process according to claim 1 , wherein:

the process comprises a total of at least 10 and up to 20 batch reactions in which in each batch reaction, the recycled dibutyltin oxide from the previous reaction is used in combination with fresh dibutyltin oxide as catalyst according claim 1 ;

in the second and/or in the subsequent batch reaction , at least 90% by weight of the recycled dibutyltin oxide recovered from the previous reaction is used with fresh dibutyltin oxide as catalyst of the subsequent reaction;

in each subsequent batch reaction, the mass ratio of recycled dibutyltin oxide and fresh dibutyltin oxide, added in the initial charge of each of the subsequent reaction is comprised between 95/5 and 87/13; and

the mass ratio of recycled dibutyltin oxide and fresh dibutyltin oxide, in the composition continuously added to compensate the azeotropic distillation in order to keep the volume constant in the reactor in case of comprising dibutyltin oxide, is comprised between 90/10 and 10/90.

17. The process according to claim 2 , wherein:

the process comprises a total of at least 3, and up to 20 batch reactions in which in each batch reaction, the recycled dibutyltin oxide from the previous reaction is used in combination with fresh dibutyltin oxide as catalyst;

the solvent is an alkane from C6 to C12, linear, cyclic or branched; and

the sequential batch reactions of the process are made in the same reactor.

18. The process according to claim 17 , wherein the composition comprising methyl(meth)acrylate and dimethylaminoethanol that is continuously added during the reaction to compensate the volume decrease due to the azeotropic distillation comprises methyl(meth)acrylate, dimethylaminoethanol, dibutyltin oxide and solvent.

Assignments (3)
CHANGE OF NAME Recorded Nov 6, 2023
From: SPCM SA
To: SNF GROUP
Reel/Frame 065469/0021 →
CHANGE OF NAME Recorded Dec 17, 2021
From: S.P.C.M. SA
To: SPCM SA
Reel/Frame 058423/0069 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2020
From: FAVERO, CÉDRICK; KIEFFER, JOHANN; LING, JING
To: S.P.C.M. SA
Reel/Frame 053889/0507 →
Continuity (1)
Related Publication 20210114969A1 · Apr 22, 2021