IP Library Granted Patent US 7,001,969
Granted Patent B2
US 7,001,969 · App. 11/018,691 · Granted Feb 21, 2006

Methods of making intermediates from polyhydroxyalkanoates

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Quick Facts
Patent No.
US 7,001,969
App. No.
11/018,691
Granted
Feb 21, 2006
Kind
B2
Abstract

Methods of forming intermediates from PHAs are disclosed.

Claims (42)

1. A method for forming an alkenoic amide, comprising:

treating a PHA to form the alkenoic amide,

wherein the alkenoic amide is derived from only one repeat unit of the PHA, and the PHA is selected from the group consisting of poly 3-hydroxypropionate, poly 2-methyl-3-hydroxypropionate, and a copolymer thereof.

2. The method of claim 1 , wherein the PHA is poly 3-hydroxypropionate.

3. The method of claim 1 , wherein the PHA is poly 2-methyl-3-hydroxypropionate.

4. The method of claim 1 , wherein the alkenoic amide is acrylamide.

5. The method of claim 1 , wherein the alkenoic amide is methacrylamide.

6. The method of claim 1 , wherein the PHA is derived from biomass selected from the group consisting of plant biomass and microbial biomass.

7. The method of claim 1 , further comprising contacting the PHA with an amine.

8. The method of claim 7 , wherein the amine is selected from the group consisting of ammonia, methyl amine, ethyl amine, and hydroxyethylamine.

9. The method of claim 1 , wherein treating the PHA occurs at a temperature of less than about 100° C.

10. The method of claim 1 , wherein treating the PHA occurs at a pressure of at least about 50 psig.

11. The method of claim 1 , wherein the percent yield of the alkenoic amide is at least about 50%.

12. A method for forming an alkenoic amide, comprising:

treating a biomass containing a PHA to form the alkenoic amide,

wherein the PHA is selected from the group consisting of poly 3-hydroxypropionate, poly 2-methyl-3-hydroxypropionate, and a copolymer thereof.

13. The method of claim 12 , wherein the alkenoic amide is acrylamide.

14. The method of claim 12 , wherein the alkenoic amide is methacrylamide.

15. The method of claim 12 , wherein the biomass is selected from the group consisting of plant biomass and microbial biomass.

16. The method of claim 12 , wherein the biomass comprises non-lyophilized biomass.

17. The method of claim 12 , further comprising contacting the PHA with an amine.

18. The method of claim 17 , wherein the amine is selected from the group consisting of ammonia, methyl amine, ethyl amine, and hydroxyethylamine.

19. A method for forming an alkenoic amide, comprising:

heating a PHA to a temperature of at most about 100° C to form the alkenoic amide,

wherein a percent yield of the alkenoic amide is at least about 50%, and the PHA is selected from the group consisting of poly 3-hydroxypropionate, poly 2-methyl-3-hydroxypropionate, and a copolymer thereof.

20. The method of claim 19 , wherein the percent yield of the alkenoic amide is at least about 60%.

21. The method of claim 19 , wherein the percent yield of the alkenoic amide is at least about 70%.

22. The method of claim 19 , wherein the percent yield of the alkenoic amide is at least about 80%.

23. The method of claim 19 , wherein the percent yield of the alkenoic amide is at least about 90%.

24. The method of claim 19 , wherein the temperature is at least about 50° C.

25. The method of claim 19 , wherein the temperature is at least about 60° C.

26. The method of claim 19 , wherein the temperature is at most about 80° C.

27. The method of claim 19 , wherein the PHA is derived from a biomass selected from the group consisting of plant biomass and microbial biomass.

28. The method of claim 19 , further comprising contacting the PHA with an amine.

29. The method of claim 28 , wherein the amine is selected from the group consisting of ammonia, methyl amine, ethyl amine, and hydroxyethylamine.

30. A method for forming an alkenoic amide, comprising:

heating a PHA to form the alkenoic amide,

wherein the PHA is selected from the group consisting of poly 3-hydroxypropionate, poly 2-methyl-3-hydroxypropionate, and a copolymer thereof.

31. The method of claim 30 , wherein the alkenoic amide is acrylamide.

32. The method of claim 30 , wherein the alkenoic amide is methacrylamide.

33. The method of claim 30 , further comprising contacting the PHA with an amine.

34. The method of claim 33 , wherein the amine is selected from the group consisting of ammonia, methyl amine, ethyl amine, and hydroxyethylamine.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2017
From: CJ RESEARCH CENTER LLC
To: CJ CHEILJEDANG CORPORATION
Reel/Frame 043723/0517 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 3, 2017
From: METABOLIX, INC.
To: CJ RESEARCH CENTER LLC
Reel/Frame 041234/0890 →
ADDRESS CHANGE Recorded May 2, 2016
From: METABOLIX, INC.
To: METABOLIX, INC.
Reel/Frame 038665/0359 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 6, 2005
From: ZHONG, LUHUA; MULLER, EDWARD M.; BARBER, JAMES J.; PUGACH, JOSEPH
To: METABOLIX INC.
Reel/Frame 016855/0352 →