IP Library Granted Patent US 8,586,793
Granted Patent B2
US 8,586,793 · App. 11/922,687 · Granted Nov 19, 2013

Process for the reductive amination of aldehydes and ketones via the formation of macrocyclic polyimine intermediates

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 8,586,793
App. No.
11/922,687
Granted
Nov 19, 2013
Kind
B2
Abstract

Aldehyde or ketone compounds having more than one carbonyl group are reductively aminated to form a product amine compound having more than one primary amino group. The aldehyde or ketone compound is reacted with the product amine compound, to form a reaction mixture that contains one or more intermediates. The intermediate is then reductively aminated to form the desired product. This process produces the desired product in very high yields with low levels of secondary amine impurities.

Claims (6)

1. A method for reductively aminating 1,3-cyclohexanedicarboxaldehyde, 1,4-cyclohexanedicarboxaldehyde, or a mixture thereof to form 1,3-bis(aminomethyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane or a mixture thereof, comprising

a) mixing 1,3-bis(aminomethyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane or a mixture thereof and 1,3-cyclohexanedicarboxaldehyde, 1,4-cyclohexanedicarboxaldehyde, or a mixture thereof at a molar ratio of at least about 1:1 but not greater than a 50% molar excess of the product amine to form a liquid mixture, and maintaining said liquid mixture at a temperature of about 0 to about 50° C. for a period of at least 5 minutes to form an intermediate mixture containing reaction intermediates wherein at at least 50% by weight of the reaction intermediates formed are macrocyclic polyimines having molecular weights of about 450 to about 1500;

b) thereafter subjecting the intermediate mixture to reductive amination conditions in the presence of ammonia and hydrogen to form 1,3-bis(aminomethyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane or a mixture thereof.

2. The method of claim 1 , wherein the concentration of 1,3-cyclohexanedicarboxaldehyde, 1,4-cyclohexanedicarboxaldehyde, or a mixture thereof in the liquid mixture is from 10 to 30% by weight, based on the combined weights of 1,3-cyclohexanedicarboxaldehyde, 1,4-cyclohexanedicarboxaldehyde, or a mixture thereof; 1,3-bis(aminomethyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane or a mixture thereof used in step a); and any solvent as may be present.

3. The method of claim 1 wherein the yield to 1,3-bis(aminomethyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane or a mixture thereof is at least 90%.

4. The method of claim 2 wherein the yield to 1,3-bis(aminomethyl)cyclohexane, 1,4-bis(aminomethyl)cyclohexane or a mixture thereof is at least 90%.

Assignments (2)
CHANGE OF NAME Recorded Mar 10, 2011
From: DOW GLOBAL TECHNOLOGIES INC.
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 025932/0093 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2007
From: TULCHINSKY, MICHAEL LEO; FISH, BARRY B.
To: DOW GLOBAL TECHNOLOGIES, INC.
Reel/Frame 020315/0106 →