IP Library Granted Patent US 9,233,908
Granted Patent B2
US 9,233,908 · App. 13/383,361 · Granted Jan 12, 2016

Cycloaliphatic diamines and method of making the same

Inventors: Abraham D. Schuitman (Midland, MI); Shawn D. Feist (Midland, MI); Barry B. Fish (Lake Jackson, TX); Daniel A. Hickman (Midland, MI); Erich J. Molitor (Midland, MI); Michael L. Tulchinsky (Midland, MI)
Assignee: Dow Global Technologies LLC
C07C209/48C07C209/26C07C2101/14
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Quick Facts
Patent No.
US 9,233,908
App. No.
13/383,361
Granted
Jan 12, 2016
Kind
B2
Abstract

The instant invention provides cycloaliphatic diamines and a method of making the same. The cycloaliphatic diamines according to the instant invention comprise the reaction product of one or more cycloaliphatic cyanoaldehydes selected from the group consisting of 1,3-cyanocyclohexane carboxaldehyde, 1,4-cyanocyclohexane carboxaldehyde, mixtures thereof, and combinations thereof, hydrogen, and ammonia fed into a continuous reductive amination reactor system; wherein the one or more cycloaliphatic cyanoaldehydes, hydrogen, and ammonia are contacted with each other in the presence of one or more heterogeneous metal based catalyst systems at a temperature in the range of from 80° C. to about 160° C. and a pressure in the range of from 700 to 3500 psig; and wherein one or more cycloaliphatic diamines are formed; and wherein said one or more cycloaliphatic diamines are selected from the group consisting of 1,3-bis(aminomethyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane, combinations thereof, and mixtures thereof.

Claims (13)

1. A process for producing cycloaliphatic diamines comprising the steps of:

feeding one or more cycloaliphatic cyanoaldehydes selected from the group consisting of 3-cyanocyclohexane-1-carboxaldehyde, 4-cyanocyclohexane-1-carboxaldehyde, mixtures thereof, and combinations thereof, hydrogen, and ammonia into a reductive amination reactor system;

contacting said one or more cycloaliphatic cyanoaldehydes, hydrogen, and ammonia with each other in the presence of one or more heterogeneous metal based catalyst systems at a temperature in the range of from 80° C. to about 160° C. and a pressure in the range of from 700 to 3500 psig, wherein said catalyst system has a space velocity in the range of from 0.1 to 5.0 per hour, wherein space velocity is defined as the ratio of the mass of the mixture of one or more cycloaliphatic cyanoaldehydes to the mass of catalyst per hour;

thereby forming one or more cycloaliphatic diamines, wherein said one or more cycloaliphatic diamines are diamines selected from the group consisting of 1,3-bis(aminomethyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane, combinations thereof, and mixtures thereof.

2. The process according to claim 1 , wherein said reductive amination reactor system comprises one or more continuous reactors in series, in parallel, or combinations thereof.

3. The process according to claim 1 , wherein said one or more heterogeneous metal based catalyst systems comprises a metal selected from the group consisting of Co, Ni, Ru, Fe, Cu, Re, Pd, oxides thereof, mixtures thereof, and combinations thereof.

4. The process according to claim 1 , wherein said one or more heterogeneous metal based catalyst systems is a bulk metal catalyst system, sponge-metal catalyst system, supported metal catalyst system, mixtures thereof, or combinations thereof.

5. The process according to claim 1 , wherein said one or more heterogeneous metal based catalyst systems comprises a bulk Co based catalyst system.

6. The process according to claim 1 , wherein said one or more heterogeneous metal based catalyst systems further comprises one or more promoters or one or more binding agents.

7. The process according to claim 6 , wherein said one or more promoters are selected from the group consisting of alkali metals and alkaline earth metals.

8. The process according to claim 6 , wherein said one or more binding agents comprise silicon oxide, aluminum oxide, titanium oxide, zirconium oxide, mixtures thereof, or combinations thereof.

9. The process according to claim 1 , wherein the catalyst lifetime facilitates a weight ratio of said one or more cycloaliphatic diamines to said one or more heterogeneous metal based catalyst systems that is greater than 300.

10. A method of improving the production yield of cycloaliphatic diamines comprising the steps of: contacting one or more cycloaliphatic cyanoaldehydes selected from the group consisting of 1,3-cyanocyclohexane carboxaldehyde, 1,4-cyanocyclohexane carboxaldehyde, mixtures thereof, and combinations thereof, hydrogen, and ammonia with each other in the presence of one or more heterogeneous metal based catalyst systems at a temperature in the range of from 80° C. to about 160° C. and a pressure in the range of from 1400 to 2500 psig, wherein said catalyst system has a space velocity in the range of from 0.1 to 5.0 per hour, wherein space velocity is defined as the ratio of the mass of the mixture of one or more cycloaliphatic cyanoaldehydes to the mass of catalyst per hour; thereby improving the product yield of one or more cycloaliphatic diamines, wherein said one or more cycloaliphatic diamines are diamines selected from the group consisting of 1,3-bis(aminomethyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane, combinations thereof, and mixtures thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2014
From: SCHUITMAN, ABRAHAM D.; FEIST, SHAWN D.; FISH, BARRY B.; HICKMAN, DANIEL A.; MOLITOR, ERICH J.; TULCHINSKY, MICHAEL L.
To: DOW GLOBAL TECHNOLOGIES INC.
Reel/Frame 032181/0596 →
CHANGE OF NAME Recorded Feb 10, 2014
From: DOW GLOBAL TECHNOLOGIES INC.
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 032192/0108 →
Continuity (2)
Provisional Application 61230319 · Jul 31, 2009
Related Publication 20120123165A1 · May 17, 2012