# US 5,710,295 A · Preparation of alkali metal acyl amino acids

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- Number: US 5,710,295 A
- Document ID: US5710295A
- Status: Granted
- Kind: A
- Application number: 08/466,094
- Filed: 1995-06-06
- Granted: 1998-01-20
- Earliest claimed: 1995-06-06
- Assignees: Hampshire Chemical Corp.
- Inventors: Richard P. Woodbury; Roger R. Gaudette; F. David Wood
- Web page: https://patentgrep.com/patent/US5710295A

## CPC

- C07C 231/02: from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
- C07C 233/49: having the carbon atom of the carboxamide group bound to a carbon atom of an acyclic unsaturated carbon skeleton
- C07C: ACYCLIC OR CARBOCYCLIC COMPOUNDS

## Abstract

A process of preparing alkali metal N-acyl amino acids, especially sodium N-acyl sarcosinates. The process of the invention eliminates the use of phosphorus trichloride or thionyl chloride and carboxylic acid chlorides. The process involves reacting the alkali metal N-acyl amino acid directly with a fatty acid at elevated temperatures with constant removal of water generated in the reaction.

## Claims

### Claim 1

A process for producing alkali metal N-acyl amino acid, comprising reacting a fatty acid having the formula RCOOH wherein R is a C.sub.1 or higher hydrocarbyl substituent with (a) an alkali metal amino acid in which the amino group is substituted with at least one hydrogen atom, and (b) the acid of said alkali metal amino acid.

### Claim 2 (depends on 1)

The process of claim 1, wherein said fatty acid is selected from the group consisting of oleic acid, lauric acid, myristic acid, coconut acid, stearic acid, nonanoic acid, decanoic acid and undecanoic acid.

### Claim 3 (depends on 1)

The process of claim 1, wherein said fatty acid is lauric acid.

### Claim 4 (depends on 1)

The process of claim 1, further comprising continuously removing water from the reaction medium as it is formed.

### Claim 5 (depends on 4)

The process of claim 4, wherein said water is removed by sparging with an inert gas.

### Claim 6 (depends on 1)

The process of claim 1, wherein the reaction is carried out at a temperature of from 170.degree. C. to 190.degree. C.

### Claim 7 (depends on 1)

The process of claim 1, wherein said acid of said alkali metal amino acid is added in an amount of one equivalent excess based upon said fatty acid.

### Claim 8 (depends on 1)

The process of claim 1, wherein said acid of said alkali metal amino acid is added in an amount of two equivalents excess based upon said fatty acid.

### Claim 9 (depends on 1)

The process of claim 1, wherein said alkali metal amino acid is selected from the group consisting of alkali metal sarcosine, alkali metal glycine, alkali metal iminodiacetic acid, alkali metal alanine, alkali metal N-methylalanine, alkali metal .beta.-alanine, alkali metal N-methyl-.beta.-alanine, alkali metal aspartic acid, alkali metal N-methyl aspartic acid, alkali metal valine, alkali metal leucine, alkali metal isoleucine, alkali metal cystine, alkali metal methionine, alkali metal phenylalanine, alkali metal glutamic acid, alkali metal proline, and alkali metal lysine.