# US 8,785,685 B2 · Process for preparing aminopolycarboxylates proceeding from amino acids

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- Number: US 8,785,685 B2
- Document ID: US8785685B2
- Status: Granted
- Kind: B2
- Application number: 13/430,105
- Filed: 2012-03-26
- Published: 2012-10-18
- Granted: 2014-07-22
- Earliest claimed: 2011-04-12
- Assignees: BASF SE
- Applicants: Robert Baumann; Markus Christian Biel; Axel Franzke; Thomas Heidenfelder; Paul Klingelhoefer; Alfred Oftring
- Inventors: Robert Baumann; Markus Christian Biel; Axel Franzke; Thomas Heidenfelder; Paul Klingelhoefer; Alfred Oftring
- Web page: https://patentgrep.com/patent/US8785685B2

## CPC

- C07C 227/18: by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters
- C07C 227/02: Formation of carboxyl groups in compounds containing amino groups, e.g. by oxidation of amino alcohols
- C07C 227/12: Formation of amino and carboxyl groups
- C07C: ACYCLIC OR CARBOCYCLIC COMPOUNDS

## Abstract

The present invention relates to a process for preparing aminopolycarboxylates proceeding from an amino acid which, in a first process step is reacted with ethylene oxide to give an intermediate mixture comprising the corresponding dialkanolamine, and then the intermediate mixture, in a second process step is converted catalytically using a base to the corresponding aminopolycarboxylate, wherein the amino acid, before the reaction with ethylene oxide in the first process step, is supplied to a partial neutralization with 0.70 to 0.99 equivalent of base per acid group, or, in the first process step, an amino acid which has already been partly neutralized with 0.70 to 0.99 equivalent of base per acid group is used.

## Claims

### Claim 1

A process for preparing an aminopolycarboxylate from an amino acid, the process comprising:
reacting the amino acid with ethylene oxide to obtain an intermediate mixture comprising dialkanolamine, and
catalytically converting the intermediate mixture with a base to an aminopolycarboxylate,
wherein the amino acid, before the reacting is partially neutralized with from 0.70 to 0.99 equivalent of base per acid group, or, in the reacting, an amino acid which has already been partially neutralized with from 0.70 to 0.99 equivalent of base per acid group is provided.

### Claim 2 (depends on 1)

The process according to claim 1,
wherein the amino acid is of formula:
wherein R is an alkyl, alkenyl, alkynyl, aryl, aralkyl, hydroxyalkyl, hydroxyaralkyl, alkylenecarboxyl or alkylenesulfonate radical and
X is an alkali metal, alkaline earth metal, hydrogen or any combination thereof.

### Claim 3 (depends on 2)

The process according to claim 2,
wherein R is a linear or branched alkyl radical having 1 to 30 carbon atoms and optionally also comprises rings, a linear or branched alkenyl radical having 2 to 30 carbon atoms and optionally also comprises rings, a linear or branched hydroxyalkyl radical having 1 to 30 carbon atoms, an alkylenecarboxylate radical having 2 to 30 carbon atoms or an alklyenesulfonate radical having 1 to 30 carbon atoms.

### Claim 4 (depends on 3)

The process according to claim 3,
wherein the amino acid is selected from the group consisting of alanine, glutamic acid, and serine.

### Claim 5 (depends on 1)

The process according to claim 1,
wherein the base is a hydroxide, carbonate, or both hydroxide and carbonate of an alkali metal, alkaline earth metal, or mixture thereof.

### Claim 6 (depends on 5)

The process according to claim 5,
wherein the base is sodium hydroxide or potassium hydroxide.

### Claim 7 (depends on 6)

The process according to claim 6,
wherein the sodium hydroxide or potassium hydroxide is contacted in an aqueous solution.

### Claim 8 (depends on 1)

The process according to claim 1,
wherein the reacting is performed at a reaction temperature of from 30 to 100° C.

### Claim 9 (depends on 1)

The process according to claim 1,
wherein the reacting is performed so that a reaction temperature during the reacting varies by less than 40° C.

### Claim 10 (depends on 1)

The process according to claim 1,
wherein the reacting is performed in the presence of a protic, polar aprotic solvent, or both.

### Claim 11 (depends on 7)

The process according to claim 7,
wherein an amount of the sodium hydroxide or potassium hydroxide is 50% by mass aqueous solution.

### Claim 12 (depends on 8)

The process according to claim 8,
wherein the reacting is performed at a reaction temperature of from 60 to 90° C.

### Claim 13 (depends on 9)

The process according to claim 9,
wherein the reacting is performed so that the reaction temperature during the reacting varies by less than 25° C.

### Claim 14 (depends on 10)

The process according to claim 10, wherein the reacting is performed in the presence of water.
