Processes for the preparation of 2,5-furandicarboxylic acid and intermediates and derivatives thereof

US10851074B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10851074-B2
Application numberUS-202016841478-A
CountryUS
Kind codeB2
Filing dateApr 6, 2020
Priority dateJan 13, 2016
Publication dateDec 1, 2020
Grant dateDec 1, 2020

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  1. Title

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  5. First independent claim

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Abstract

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The present disclosure provides processes for the production of 2-5-furandicarboxylic acid (FDCA) and intermediates thereof by the chemocatalytic conversion of a furanic oxidation substrate. The present disclosure further provides processes for preparing derivatives of FDCA and FDCA-based polymers. In addition, the present disclosure provides crystalline preparations of FDCA, as well as processes for making the same.

First claim

Opening claim text (preview).

We claim: 1. A process for producing a first 2,5-furandicarboxylic acid (FDCA) pathway product from a first furanic oxidation substrate, the process comprising: (a) contacting a first oxidation feedstock comprising a first furanic oxidation substrate and a first oxidation solvent with oxygen in the presence of a first heterogeneous oxidation catalyst under conditions sufficient to form a reaction mixture for oxidizing the first furanic oxidation substrate to a first FDCA pathway product, and producing the first FDCA pathway product; wherein the first oxidation solvent is a multi-component solvent comprising water and a water-miscible aprotic organic solvent; wherein no base is added to the reaction mixture during (first) contacting step (a); wherein the first oxidation feedstock has a pH of less than about 6; wherein the first heterogeneous oxidation catalyst comprises a first solid support and a first noble metal, and wherein the first solid support comprises a specific surface area in the range of from or any number in between 20 m 2 /g to 100 m 2 /g. 2. The process of claim 1 , wherein the first noble metal is selected from the group consisting of platinum, gold, and combinations thereof. 3. The process of claim 1 , wherein the water-miscible aprotic organic solvent is selected from the group consisting of tetrahydrofuran, a glyme, dioxane, a dioxolane, dimethylformamide, dimethylsulfoxide, sulfolane, acetone, N-methyl-2-pyrrolidone (“NMP”), methyl ethyl ketone (“MEK”), and gamma-valerolactone; and, if the water-miscible aprotic organic solvent is a glyme, then the glyme is selected from the group consisting of a monoglyme (1,2-dimethoxyethane), ethyl glyme, diglyme (diethylene glycol dimethyl ether), ethyl diglyme, triglyme, butyl diglyme, tetraglyme, and a polyglyme. 4. The process of claim 3 , wherein the water-miscible aprotic organic solvent is a glyme. 5. The process of claim 4 , wherein the water-miscible aprotic organic solvent is 1,2-dimethoxyethane (“DME”). 6. The process of claim 4 , wherein the water-miscible aprotic organic solvent is diglyme. 7. The process of claim 3 , wherein the water-miscible aprotic organic solvent is dioxane. 8. The process of claim 3 , wherein the water-miscible aprotic organic solvent is NMP. 9. The process of claim 3 , wherein the water-miscible aprotic organic solvent is MEK. 10. The process of claim 1 , wherein the weight percent ratio of the water-miscible aprotic organic solvent:water is in the range of from or any number in between 70:30 to 20:80. 11. The process of claim 10 , wherein the weight percent ratio of the water-miscible aprotic organic solvent:water is in the range of from or any number in between 60:40 to 40:60. 12. The process of claim 1 , wherein the first oxidation feedstock comprises the first furanic oxidation substrate at a concentration of at least 5% by weight. 13. The process of claim 1 , wherein the first heterogeneous oxidation catalyst comprises the first noble metal at a loading in the range of from or any number in between 0.3% to 5% by weight of the first heterogeneous oxidation catalyst. 14. The process of claim 1 , wherein the first solid support comprises a material selected from the group consisting of a metal oxide, a carbonaceous material, a polymer, a metal silicate, a metal carbide, and any combination of two or more thereof. 15. The process of claim 1 , wherein the first solid support comprises a plurality of pores. 16. The process of claim 15 , wherein the first solid support comprises a pore volume wherein at least 50% of the pore volume is from pores having a pore diameter in the range of from or any number in between 5 nm to 100 nm. 17. The process of claim 1 , wherein the first solid support comprises a specific surface area of about 25 m 2 /g. 18. The process of claim 1 , wherein the first solid support comprises a specific surface area of about 20 m 2 /g. 19. The process of claim 1 , wherein the first solid support comprises a specific surface area in the range of from or any number in between 20 m 2 /g to 30 m 2 /g. 20. The process of claim 1 , wherein oxygen is present at a molar ratio of oxygen:the first furanic oxidation substrate in the range of from or any number in between 2:1 to 10:1. 21. The process of claim 1 , wherein (first) contacting step (a) is carried out at a temperature in the range of from or any number in between 50° C. to 200° C. 22. The process of claim 1 , wherein the first FDCA pathway product is produced at a yield of at least 80%. 23. The process of claim 1 , wherein the first FDCA pathway product is FDCA. 24. The process of claim 1 , wherein the first oxidation feedstock has a pH of about 3-6. 25. The process of claim 1 , further comprising a second oxidation step, wherein the second oxidation step comprises: (b) contacting a second oxidation feedstock comprising a second furanic oxidation substrate and a second oxidation solvent with oxygen in the presence of a second heterogeneous oxidation catalyst under conditions sufficient to form a second reaction mixture for oxidizing the second furanic oxidation substrate to produce a second FDCA pathway product, and producing the second FDCA pathway product; wherein the first FDCA pathway product is an FDCA pathway intermediate compound, either alone or together with FDCA; wherein the second furanic oxidation substrate is the first FDCA pathway product; and wherein the second heterogeneous oxidation catalyst comprises a second solid support and a second noble metal, that may be the same or different from the first noble metal. 26. The process of claim 25 , wherein the second noble metal is selected from the group consisting of platinum, gold, and a combination thereof. 27. The process of claim 25 , wherein the second solid support comprises a plurality of pores. 28. The process of claim 25 , wherein the second solid support comprises a specific surface area in the range of from or any number in between 20 m 2 /g to 100 m 2 /g. 29. The process of claim 25 , wherein the second solid support comprises a specific surface area in the range of from or any number in between 20 m 2 /g to 30 m 2 /g. 30. The process of claim 1 , further comprising: (a o ) prior to (first) contacting step (a), contacting a carbohydrate feedstock comprising a sugar and a dehydration solvent with a dehydration catalyst under conditions sufficient to form a dehydration reaction mixture for dehydrating the sugar to produce the first furanic oxidation substrate, wherein the first furanic oxidation substrate is present in a dehydration product solution that comprises the first furanic oxidation substrate and the dehydration solvent. 31. The process of claim 30 , wherein the dehydration catalyst is an acid catalyst. 32. The process of claim 31 , wherein the acid catalyst is an acid selected from the group consisting of HBr, H 2 SO 4 , HNO 3 , HCl, HI, H 3 PO 4 , triflic acid, methansulfonic acid, benzenesulfonic acid, and p-toluene sulfonic acid. 33. The process of claim 32 , wherein the acid catalyst is HCl. 34. The process of claim 30 , wherein the dehydration solvent comprises 1,4-dioxane and water. 35. The process of claim 30 , wherein the sugar is fructose and the first furanic

Assignees

Inventors

Classifications

  • B01J8/02Primary

    with stationary particles, e.g. in fixed beds · CPC title

  • C07D307/68Primary

    Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen · CPC title

  • Gold · CPC title

  • Platinum · CPC title

  • Recycling of unreacted starting or intermediate materials · CPC title

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What does patent US10851074B2 cover?
The present disclosure provides processes for the production of 2-5-furandicarboxylic acid (FDCA) and intermediates thereof by the chemocatalytic conversion of a furanic oxidation substrate. The present disclosure further provides processes for preparing derivatives of FDCA and FDCA-based polymers. In addition, the present disclosure provides crystalline preparations of FDCA, as well as process…
Who is the assignee on this patent?
Stora Enso Oyj
What technology area does this patent fall under?
Primary CPC classification B01J8/02. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Dec 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).