IP Library Granted Patent US 8,367,819
Granted Patent B2
US 8,367,819 · App. 13/175,450 · Granted Feb 5, 2013

Synthesis of caprolactam from lysine

Inventor: John W. Frost (Okemos, MI)
Assignee: Board of Trustees of Michigan State University
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Quick Facts
Patent No.
US 8,367,819
App. No.
13/175,450
Granted
Feb 5, 2013
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-εcaprolactam, 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 (16)

1. A method for producing α-amino-ε-caprolactam, the method comprising:

(A) providing a lysine derived from a biomass; and

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

2. A method according to claim 1 , wherein the lysine comprises L-lysine derived from the 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 includes using a fermentation reaction to convert the sugar into L-lysine.

5. A method according to claim 1 further comprising converting the biomass into lactic acid.

6. A method according to claim 5 further comprising hydrogenating the lactic acid to produce 1,2-propanediol.

7. A method according to claim 6 further comprising using the 1,2-propanediol as the alcohol in the heating step (B).

8. A method according to claim 1 , wherein in the heating step (B) the lysine is in the form of a hydrochloride, monophosphate or diphosphate salt.

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

10. A method according to claim 9 , wherein the alcohol includes a diol or triol.

11. A method according to claim 9 , wherein the alcohol includes a glycol.

12. A method according to claim 9 , wherein the alcohol includes ethanol, 1-propanol, 1-butanol, 1-pentanol, 1-hexanol, 1,2-propanediol, or mixtures thereof.

13. A method according to claim 12 , wherein the alcohol is 1,2-propanediol.

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

Assignments (1)
SECURITY AGREEMENT Recorded Nov 9, 2011
From: MERCHSOURCE, LLC (AS GRANTOR)
To: GENERAL ELECTRIC CAPITAL CORPORATION (AS GRANTEE)
Reel/Frame 027211/0958 →
Continuity (5)
Continuation 12147256 · Jun 26, 2008
Division 11635373 · Dec 7, 2006
Continuation PCTUS2005020326 · Jun 9, 2005
Provisional Application 60578620 · Jun 10, 2004
Related Publication 20120142886A1 · Jun 7, 2012