IP Library Granted Patent US 8,394,992
Granted Patent B2
US 8,394,992 · App. 13/269,399 · Granted Mar 12, 2013

Synthesis of triethylenetetramines

Inventors: Marco Jonas (Neuenhof, CH); Irene Vaulont (Buchs, CH); Antonio Soi (Buchs AG, CH); Gunther Schmidt (Aarau, CH)
Assignee: PhilEra New Zealand Limited
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Quick Facts
Patent No.
US 8,394,992
App. No.
13/269,399
Granted
Mar 12, 2013
Kind
B2
Abstract

Methods and intermediates for synthesizing triethylenetetramine and salts thereof, as well as novel triethylenetetramine salts and their crystal structure, and triethylenetetramine salts of high purity.

Claims (17)

1. A process for preparing triethylenetetramine dihydrochloride, comprising: (a) reacting triethylenetetramine tetrahydrochloride with a base in a solvent to produce triethylenetetramine and chloride salt; (b) removing said chloride salt from solution; (c) reacting said triethylenetetramine with about 2 equivalents of concentrated hydrochloric acid to form triethylenetetramine dihydrochloride; and (d) adding an alcohol to the solution and precipitating said triethylenetetramine dihydrochloride.

2. The process of claim 1 , wherein the base is sodium methoxide or sodium ethoxide.

3. The process of claim 1 , wherein the solvent is ethanol or methanol.

4. The process of claim 1 , wherein the removal in step (b) of the chloride salt is by precipitation.

5. The process of claim 4 , wherein the precipitate is removed by filtration.

6. The process of claim 4 , wherein the precipitate is washed with a solvent.

7. The process of claim 6 , wherein the solvent is tert-butylmethylether.

8. The process of claim 1 , wherein the acid has been pre-dissolved in a solvent prior to its addition to the free triethylenetetramine.

9. The process of claim 1 , wherein the alcohol is ethanol, methanol, or isopropanol.

10. The process of claim 1 , wherein about 4 equivalents of sodium methoxide are mixed with about 1 equivalent of triethylenetetramine tetrahydrochloride.

11. The process of claim 10 , wherein the triethylenetetramine tetrahydrochloride is in a mixture of methanol and ethanol.

12. The process of claim 1 , wherein the triethylenetetramine dihydrochloride product precipitates in yield greater than about 86%.

13. The process of claim 1 , wherein purity of the triethylenetetramine dihydrochloride product is about 100%, as determined using the methods set forth in USP27-NF22 (page 1890) for analysis of trientine.

14. The process of claim 13 , wherein the triethylenetetramine dihydrochloride product has less than about 10 ppm heavy metals as determined by USP <231> II.

15. The process of claim 1 , wherein precipitating said triethylenetetramine dihydrochloride in step (d) comprises adding seed crystals of triethylenetetramine dihydrochloride.

16. The process of claim 1 , wherein said triethylenetetramine dihydrochloride is crystalline.

17. The process of claim 16 , wherein said crystalline triethylenetetramine dihydrochloride is a thermodynamic polymorph.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2011
From: JONAS, MARCO; VAULONT, IRENE; SOI, ANTONIO; SCHMIDT, GUNTHER
To: PROTEMIX CORPORATION LIMITED
Reel/Frame 027051/0875 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2011
From: PROTEMIX CORPORATION LIMITED
To: PHILERA NEW ZEALAND LIMITED
Reel/Frame 027051/0894 →
Continuity (4)
Continuation 12460616 · Jul 21, 2009
Division 11184761 · Jul 19, 2005
Provisional Application 60589080 · Jul 19, 2004
Related Publication 20120029203A1 · Feb 2, 2012