IP Library Granted Patent US 7,977,450
Granted Patent B2
US 7,977,450 · App. 12/147,256 · Granted Jul 12, 2011

Synthesis of caprolactam from lysine

Assignee: Board of Trustees of Michigan State University
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Quick Facts
Patent No.
US 7,977,450
App. No.
12/147,256
Granted
Jul 12, 2011
Kind
B2
Abstract

In various embodiments, the present invention can involve a method of synthesizing α-amino-ε-caprolactam. The method can comprise heating a salt of L-lysine in a solvent comprising an alcohol. In other embodiments, the present invention can involve methods for synthesizing ε-caprolactam. The methods can comprise heating a salt of L-lysine in a solvent comprising an alcohol and deaminating the reaction product. In various embodiments, the invention can include methods of converting biomass into nylon 6. The methods can comprise heating L-lysine in a solvent comprising an alcohol to produce α-amino-ε-caprolactam, deaminating to produce ε-caprolactam and polymerizing into nylon 6, wherein the L-lysine is derived from the biomass. In other embodiments, the present invention can include methods of making nylon 6. The methods can comprise synthesizing ε-caprolactam and then polymerizing, wherein the ε-caprolactam is derived from L-lysine.

Claims (21)

1. A method for producing nylon 6, the method comprising:

(A) heating lysine in a solvent comprising an alcohol, at a temperature of about 99° C. to about 201° C., to produce α-amino-ε-caprolactam;

(B) deaminating α-amino-ε-caprolactam produced in (A) by a method comprising contacting it at least once with a deamination reagent or catalyst at a temperature below the freezing point of water, to produce ε-caprolactam; and

(C) polymerizing ε-caprolactam produced in (B) into nylon 6.

2. A method according to claim 1 , wherein the lysine comprises L-lysine derived from biomass.

3. A method according to claim 2 , wherein the L-lysine is derived by obtaining a sugar from the biomass and converting the sugar into L-lysine.

4. A method according to claim 3 , wherein the converting comprises using a fermentation reaction to convert the sugar into L-lysine.

5. A method according to claim 4 further comprising recycling an amine, produced by deamination of α-amino-ε-caprolactam, into the fermentation reaction.

6. A method according to claim 2 further comprising creating lactic acid from the biomass.

7. A method according to claim 6 further comprising hydrogenating the lactic acid to produce 1,2-propanediol.

8. A method according to claim 7 further comprising using the 1,2-propanediol as the alcohol in the heating step (A).

9. A method according to claim 1 , wherein the heating (A) comprises heating in the presence of a catalyst.

10. A method according to claim 1 , wherein the alcohol used in the heating step (A) has from 2 to 6 carbons.

11. A method according to claim 10 , wherein the alcohol comprises a diol.

12. A method according to claim 10 , wherein the alcohol comprises a triol.

13. A method according to claim 10 , wherein the alcohol comprises a glycol.

14. A method according to claim 10 , wherein the alcohol is from the group consisting of ethanol, 1-propanol, 1-butanol, 1-pentanol, 1-hexanol, 1,2-propanediol, and mixtures thereof.

15. A method according to claim 14 , wherein the alcohol is 1,2-propanediol.

16. A method according to claim 1 , wherein the heating is below the temperature of polymerization of caprolactam.

17. A method according to claim 1 , wherein the heating allows the azeotropic removal of water.

18. A method according to claim 1 , wherein the heating is accomplished by reflux.

Assignments (2)
CONFIRMATORY LICENSE Recorded Apr 10, 2015
From: MICHIGAN STATE UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 035411/0801 →
CONFIRMATORY LICENSE Recorded May 14, 2010
From: MICHIGAN STATE UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 024384/0651 →
Continuity (4)
Division 11635373 · Dec 7, 2006
Continuation PCTUS2005020326 · Jun 9, 2005
Provisional Application 60578620 · Jun 10, 2004
Related Publication 20090005532A1 · Jan 1, 2009