IP Library Granted Patent US 7,405,325
Granted Patent B2
US 7,405,325 · App. 11/788,064 · Granted Jul 29, 2008

Process for the preparation of 4-hydroxalkylamino-2-nitro-anisoles

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Quick Facts
Patent No.
US 7,405,325
App. No.
11/788,064
Granted
Jul 29, 2008
Kind
B2
Abstract

A process for the preparation of 4-hydroxyalkylamino-2-nitro-anisoles of the general formula (I) wherein m is 2 or 3; by reaction of a 4-halogeno-3-nitro-aniline of formula (II) with a chloroalkyl-chloroformate of formula (III), alkaline ring closure of the resulting carbamate and nucleophilic replacement of the halogeno atom by a methoxy group to form a derivative of formula (IV), and finally ring opening of the resulting cyclic carbamate by treatment with methanolic alkali metal hydroxide, followed by neutralization with inorganic or organic acids, wherein the complete reaction is executed in a non-aqueous medium; as well as process for the preparation of 2-amino-4-hydroxyalkylamino-anisoles of formula (V)

Claims (12)

1. A process for the preparation of 4-hydroxyalkylamino-2-nitro-anisoles of the general formula (I)

wherein m is 2 or 3;

wherein a 4-halogeno-3-nitro-aniline of formula (II) is caused to react with a chloroalkyl-chloroformate, followed by an alkaline ring closure of the resulting carbamate and a nucleophilic replacement of the halogeno atom by a methoxy group to form a derivative of formula (IV), and then followed by a ring opening of the resulting cyclic carbamate by a treatment with methanolic alkali metal hydroxide, and finally followed by a neutralization with an inorganic or organic acid, wherein the complete reaction is executed in a non-aqueous medium.

2. A process according to claim 1 , wherein said 4-halogeno-3-nitro-aniline of formula (II) is a 4-chloro-3-nitro-aniline or a 4-fluoro-3-nitro-aniline.

3. A process according to claim 1 , wherein said non-aqueous medium is an inert dipolar aprotic solvent.

4. A process according to claim 1 , wherein the first two reaction steps are performed at a temperature of from about 40° C. to about 60° C.

5. A process according to claim 1 , wherein said nucleophilic replacement of the halogeno atom is carried out with 3 equivalents of alkali methoxide per equivalent of said derivative of formula (IV).

6. A process according to claim 1 , wherein said alkali metal hydroxide is a sodium hydroxide or a potassium hydroxide.

7. A process for the preparation of 2-amino-4-hydroxyalkylamino-anisoles of the general formula (V)

wherein m is 2 or 3;

wherein the process according to claim 1 is followed by a reduction of said 4-hydroxyalkylamino-2-nitro-anisole of formula (I).

8. A process according to claim 7 , wherein a catalytic hydrogenation is used for the reduction of said 4-hydroxyalkylamino-2-nitro-anisole of (I).

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2021
From: NOXELL CORPORATION
To: WELLA OPERATIONS US, LLC
Reel/Frame 056339/0928 →
CORRECTIVE ASSIGNMENT TO CORRECT THE THE NAME OF ASSIGNOR PREVIOUSLY RECORDED ON REEL 040437 FRAME 0133. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Dec 15, 2016
From: THE PROCTER AND GAMBLE COMPANY
To: GALLERIA CO.
Reel/Frame 040941/0637 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2016
From: GALLERIA CO.
To: NOXELL CORPORATION
Reel/Frame 040436/0438 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2016
From: PROCTER AND GAMBLE COMPANY
To: GALLERIA CO.
Reel/Frame 040437/0133 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 4, 2007
From: GOTTEL, OTTO; MORAND, EMMANUEL; BRAUN, HANS-JURGEN
To: PROCTER & GAMBLE COMPANY, THE
Reel/Frame 019377/0696 →