# US 5,710,333 A · Process for the preparation of tertiary amine oxides

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- Number: US 5,710,333 A
- Document ID: US5710333A
- Status: Granted
- Kind: A
- Application number: 08/693,915
- Filed: 1996-08-06
- Granted: 1998-01-20
- Earliest claimed: 1995-08-07
- Assignees: Hoechst Aktiengesellschaft
- Inventors: Georg Bader; Ramon Joglar Tamargo
- Web page: https://patentgrep.com/patent/US5710333A

## CPC

- C07C 291/04: containing amino-oxide bonds
- C07C: ACYCLIC OR CARBOCYCLIC COMPOUNDS

## Abstract

Process for the preparation of tertiary amine oxides by reaction of a tertiary amine with a compound which splits off oxygen. To avoid gel and foam formation, a portion of the amine oxide to be prepared is added before the start of this reaction.

## Claims

### Claim 1

A process for the preparation of a tertiary amine oxide of the formula I ##STR2## in which R.sup.1 is C.sub.1 -C.sub.3 -alkyl,
R.sup.2 is C.sub.1 -C.sub.20 -alkyl and
R.sup.3 is C.sub.6 -C.sub.22 -alkyl,
by reaction of a tertiary amine of the formula II
R.sup.1 R.sup.2 R.sup.3 N (II)
with a compound which splits off oxygen, which comprises carrying out the reaction in the presence of 1 to 15% by weight, based on the reaction mixture of a tertiary amine oxide of the formula I wherein essentially all of said tertiary amine oxide is present in the reaction mixture before the reaction starts.

### Claim 2 (depends on 1)

The process as claimed in claim 1, wherein the preparation is carried out in the presence of the tertiary amine oxide to be prepared.

### Claim 3 (depends on 1)

The process as claimed in claim 1, wherein R.sup.1 is methyl or ethyl, R.sup.2 is C.sub.1 -C.sub.12 -alkyl and R.sup.3 is C.sub.8 -C.sub.20 -alkyl.

### Claim 4 (depends on 1)

The process as claimed in claim 1, wherein hydrogen peroxide, alkali metal hypochlorite, an inorganic peracid or an organic peracid is employed as the compound which splits off oxygen.

### Claim 5 (depends on 1)

The process as claimed in claim 1, wherein an aqueous hydrogen peroxide solution is employed.

### Claim 6 (depends on 1)

The process as claimed in claim 1, wherein a 3 to 90% strength by weight hydrogen peroxide solution is employed.

### Claim 7 (depends on 1)

The process as claimed in claim 1, wherein 1-1.5 mol of hydrogen peroxide per mole of amine of the formula II are employed.

### Claim 8 (depends on 1)

The process as claimed in claim 1, wherein the reaction is carried out at a temperature in the range from 0.degree. to 100.degree. C.

### Claim 9 (depends on 1)

The process claimed in claim 1, wherein a 20 to 70% strength by weight hydrogen peroxide solution is employed.

### Claim 10 (depends on 1)

The process as claimed in claim 1, wherein a 20 to 40% by weight hydrogen peroxide solution is employed.

### Claim 11 (depends on 1)

The process as claimed in claim 1, wherein 1.01-1.1 mol of hydrogen peroxide per mole of amine of the formula II are employed.

### Claim 12 (depends on 1)

The process as claimed in claim 1, wherein the reaction is carried out at a temperature in the range from 30.degree. to 90.degree. C.

### Claim 13 (depends on 1)

The process as claimed in claim 1, wherein the reaction is carried out at a temperature in the range from 45.degree. to 85 .degree. C.
