IP Library Granted Patent US 10,472,320
Granted Patent B2
US 10,472,320 · App. 15/736,372 · Granted Nov 12, 2019

Process to prepare phenolic ethylenediamine diacetic acid compounds

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,472,320
App. No.
15/736,372
Granted
Nov 12, 2019
Kind
B2
Abstract

The present invention relates to a process to prepare N,N′-di(2-hydroxybenzyl) ethylenediamine-N,N′-diacetic acid and salts thereof (HBED) comprising a reaction between formaldehyde, ethylenediamine diacetic acid or a salt thereof (EDDA) and phenol, wherein the reaction mixture contains 0.2 to 1.1 molar equivalents of alkali metal ions on the basis of the molar amount of EDDA and the reaction mixture is processed by a step in which at least part of the organic compounds other than the formed HBED are removed from the reaction mixture, and optionally recycled, during which step at least 50% and up to and including 100% of the alkali metal ions in the reaction mixture are potassium ions, to products obtainable by such process and their use.

Claims (12)

1. Process to prepare N,N′-di(2-hydroxybenzyl) ethylenediamine-N,N′-diacetic acid and salts thereof (HBED) comprising a reaction between formaldehyde, ethylenediamine diacetic acid or a salt thereof (EDDA) and phenol, wherein the reaction mixture contains 0.2 to 1.1 molar equivalents of alkali metal ions on the basis of the molar amount of EDDA and the reaction mixture is processed by a step in which at least part of the organic compounds other than the formed HBED are removed from the reaction mixture, and optionally recycled, during which step at least 50% and up to and including 100% of the alkali metal ions in the reaction mixture are potassium ions.

2. Process of claim 1 , wherein the reaction between formaldehyde, EDDA and phenol is performed at a pH of between 3 and 7 and a temperature below 60° C.

3. Process of claim 2 , wherein the 0.2-1.1 equivalent of alkali metal ions on molar amount of EDDA is obtained by the addition of alkali metal hydroxide or by adding the EDDA as an ethylenediamine diacetate alkali metal salt or in an aqueous solution containing alkali metal ions.

4. Process of claim 2 comprising a first step wherein a reaction is performed between formaldehyde and ethylenediamine diacetic acid or a salt thereof to give an adduct and a second step wherein the adduct of formaldehyde and ethylenediamine diacetic acid or a salt thereof is reacted with phenol while ensuring that the pH is between 3 and 7 and the temperature is below 60° C.

5. Process of claim 2 comprising a first step of preparing a mixture comprising phenol and ethylenediamine diacetic acid or a salt thereof and a second step of reacting this mixture with formaldehyde at a pH of between 3 and 7 and a temperature of below 60° C.

6. Process of claim 2 comprising a first step of preparing a mixture comprising phenol and formaldehyde and a second step of reacting this mixture with ethylenediamine diacetic acid or a salt thereof at a pH of between 3 and 7 and a temperature of below 60° C.

7. Process of claim 1 , wherein in a step between the reaction between EDDA, phenol and formaldehyde and the processing step further alkali metal is added to the reaction mixture.

8. Process of claim 7 , wherein the addition of further alkali metal increases the pH to a value higher than 7.

9. Process of claim 1 , wherein 60 to 100 mole % of the alkali metal in the reaction mixture during the processing step are potassium.

10. Process of claim 1 containing an additional step wherein the product is converted to the acid, another salt or metal complex.

11. Process of claim 1 containing an additional drying step.

12. Process of claim 11 , wherein the drying step is a spray drying step.

Assignments (3)
CHANGE OF NAME Recorded Sep 18, 2019
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS INTERNATIONAL B.V.
Reel/Frame 050426/0671 →
SECURITY INTEREST Recorded Oct 1, 2018
From: STARFRUIT US MERGER SUB 1 LLC; STARFRUIT US MERGER SUB 2 LLC; AKZO NOBEL SURFACE CHEMISTRY LLC; AKZO NOBEL CHEMICALS B.V.; AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: WILMINGTON TRUST (LONDON) LIMITED, AS COLLATERAL AGENT
Reel/Frame 047231/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2017
From: REICHWEIN, ADRIANUS MARIA; JONGEN, HUBERTUS JOHANNES; GROOTE, MARJOLEIN
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 044395/0869 →