Methods of making intermediates from polyhydroxyalkanoates
View Patent ↗Methods of forming intermediates from PHAs are disclosed. In general, the methods include forming a pyrrolidone from a PHA, such as poly 4-hydroxybutyrate or a 4-hydroxybutyrate containing polymer. The methods can include, for example, treating (e.g., heating) the PHA to form a pyrrolidone. The methods can include, for example, treating a biomass containing the PHA to form a pyrrolidone. The methods can include, for example, heating the PHA to a temperature of at most about 90° C. to form a pyrrolidone, wherein the percent yield of the pyrrolidone is at least about 50%.
1. A method of forming a pyrrolidone, comprising:
treating a PHA to form the pyrrolidone,
wherein the PHA is poly 4-hydroxybutyrate or a 4-hydroxybutyrate containing polymer, and the pyrrolidone has only one repeat unit from the PHA.
2. The method of claim 1 , wherein the PHA is derived from biomass selected from the group consisting of plant biomass and microbial biomass.
3. The method of claim 2 , wherein less than about 50 weight percent of the PHA that is treated to form the pyrrolidone is removed from the biomass before being treated to form the pyrrolidone.
4. The method of claim 2 , further comprising, before treating the PHA to form the pyrrolidone, removing at least about 60 weight percent of the PHA that is treated to form the pyrrolidone from the biomass.
5. The method of claim 1 , further comprising contacting the PHA with an amine.
6. The method of claim 5 , wherein the amine comprises an aliphatic amine.
7. The method of claim 5 , wherein the amine is selected from the group consisting of ammonia, methyl amine, ethyl amine and hydroxyethylamine.
8. The method of claim 1 , further comprising combining the PHA with an amine to form a combination,
wherein the combination contains less than about one milliliter of solvent other than the amine per gram of the PHA.
9. The method of claim 1 , wherein treating the PHA occurs at a temperature of less than about 90° 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 pyrrolidone is at least about 50%.
12. The method of claim 1 , further comprising combining the PHA with an amine,
wherein a ratio of moles of amine per mole of PHA monomer unit is less than bout 20.
13. The method of claim 1 , wherein the PHA is a chiral PHA, and percent chirality yield of chiral pyrrolidone is at least about five percent.
14. The method of claim 1 , wherein the pyrrolidone is N-methylpyrrolidone.
15. The method of claim 1 , wherein the pyrrolidone is N-vinylpyrrolidone.
16. The method of claim 1 , wherein the method comprises forming an acyclic amide, and heating the acyclic amide to form the pyrrolidone.
17. A method for forming a pyrrolidone, comprising:
treating a biomass containing a PHA to form the pyrrolidone,
wherein the PHA is poly 4-hydroxybutyrate or a 4-hydroxybutyrate containing polymer.
18. The method of claim 17 , wherein the biomass is selected from the group consisting of plant biomass and microbial biomass.
19. The method of claim 17 , wherein the biomass comprises non-lyophilized biomass.
20. The method of claim 17 , further comprising contacting the PHA with an amine.
21. The method of claim 20 , wherein the amine comprises an aliphatic amine.
22. The method of claim 20 , wherein the amine is selected from the group consisting of ammonia, methyl amine, ethyl amine and hydroxyethylamine.
23. The method of claim 17 , further comprising combining PHA with an amine to form a combination,
wherein the combination contains less than about one milliliter of solvent other than the amine per gram of the PHA.
24. The method of clam 17 , wherein treating the biomass occurs at a temperature of less than about 90° C.
25. The method of claim 17 , wherein treating the biomass occurs at a pressure of at least about 50 psig.
26. The method of claim 17 , wherein the percent yield of the pyrrolidone is at least about 50%.
27. The method of claim 17 , further comprising combining the PHA with an amine,
wherein a ratio of moles of amine per mole of PHA monomer unit is less than about 20.
28. The method of claim 17 , wherein the PHA is a chiral PHA, and a percent chirality yield of chiral pyrrolidone is at least about five percent.
29. The method of claim 17 , wherein the pyrrolidone is N-methylpyrrolidone.
30. The method of claim 17 , wherein the pyrrolidone is N-vinylpyrrolidone.
31. The method of claim 17 , wherein the method comprises forming an acyclic amide, and heating the acyclic amide to form the pyrrolidone.
32. A method for forming a pyrrolidone, comprising:
heating a PHA to a temperature of at most about 90° C. to form the pyrrolidone,
wherein the PHA is poly 4-hydroxybutyrate or a 4-hydroxybutyrate containing polymer, and a percent yield of the pyrrolidone is at least about 50%.
33. The method of claim 32 , wherein the percent yield of the pyrrolidone is at least about 60%.
34. The method of claim 32 , wherein the percent yield of the pyrrolidone is at least about 70%.
35. The method of claim 32 , wherein the percent yield of the pyrrolidone is at least about 80%.
36. The method of claim 32 , wherein the percent yield of the pyrrolidone is at least about 90%.
37. The method of claim 32 , wherein the temperature is at least about 50° C.
38. The method of claim 32 , wherein the temperature is at least about 60° C.
39. The method of claim 32 , wherein the temperature is at least about 70° C.
40. The method of claim 32 , wherein the PHA is derived from biomass selected from the group consisting of plant biomass and microbial biomass.
41. The method of claim 32 , wherein the pyrrolidone has only one monomer unit from the PHA.
42. A method for forming a pyrrolidone, comprising:
heating a PHA to form the pyrrolidone,
wherein the PHA is poly 4-hydroxybutyrate or a 4-hydroxybutyrate containing polymer.
43. The method of claim 42 , wherein the pyrrolidone comprises N-methylpyrrolidone or N-hydroxyethyl pyrrolidone.
44. The method of claim 42 , wherein the pyrrolidone has an integer number of carbon-carbon bonds, the integer number being selected from the group consisting of three, four, five, six, seven, eight and nine.
45. The method of claim 42 , further comprising contacting the PHA with an amine.
46. The method of claim 45 , wherein the amine is an acyclic amine.
47. The method of claim 42 , further comprising, before forming the pyrrolidone, forming an acyclic amide, and treating the acyclic amide to form the pyrrolidone.