IP Library › Granted Patent US 8,618,108
Granted Patent B2
US 8,618,108 · App. 12/587,338 · Granted Dec 31, 2013

Methods of making cyclic, N-amino functional triamines

Inventors: Stephen W. King (League City, TX); Stefan K. Mierau (South Charleston, WV); Thomas Z. Srnak (Arlington Heights, IL)
Assignee: Union Carbide Chemicals & Plastics Technology LLC
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Quick Facts
Patent No.
US 8,618,108
App. No.
12/587,338
Granted
Dec 31, 2013
Kind
B2
Abstract

The present invention provides strategies for making cyclic triamines. Reactant media including certain precursors and/or certain types of catalysts can be converted into cyclic triamines with improved conversion and selectivity. The strategies can be incorporated into reactions that involve transamination schemes and/or reductive amination schemes. In the case of transamination, for instance, using transamination to cause ring closure of higher amines in the presence of a suitable catalyst leads to desired cyclic triamines with notable conversion and yield. In the case of reductive amination, reacting suitable polyfunctional precursors in the presence of a suitable catalyst also yields cyclic triamines via ring closure with notable selectivity and conversion. Both transamination and reductive amination methodologies can be practiced under much milder temperatures than are used when solely acid catalysts are used. Preferred embodiments can produce reaction mixtures that are generally free of salt by-products.

Claims (10)

1. A method of making a cyclic triamine of the type comprising first and second nitrogen backbone atoms and an N-amino moiety pendant from at least one of the nitrogen backbone atoms, comprising the steps of:

providing a polyfunctional compound comprising at least 4 amine moieties and, optionally, one or more nitrile moieties said polyfunctional compound being selected from the group

a)

b) one or more tetramines; and

c) a polyamine having at least one nitrile moiety; and

causing ring closure of the polyfunctional compound in the presence of a transamination catalyst under conditions effective to cause the polyfunctional compound to react with itself to form the cyclic triamine.

2. The method of claim 1 , wherein the polyfunctional compound comprises one or more tetraamines.

3. The method of claim 1 , wherein the polyfunctional compound is

4. The method of claim 1 , wherein the polyfunctional compound comprises a polyamine having at least one nitrile moiety.

5. The method of claim 1 , wherein the catalyst comprises Ni and Re.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 28, 2020
From: UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY LLC
To: UNION CARBIDE CORPORATION
Reel/Frame 051642/0392 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 23, 2010
From: KING, STEPHEN W.; MIERAU, STEFAN K.; SRNAK, THOMAS Z.
To: UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY LLC
Reel/Frame 025034/0718 →
Continuity (2)
Provisional Application 61195412 · Oct 6, 2008
Related Publication 20100094007A1 · Apr 15, 2010