Biorefining compounds and organocatalytic upgrading methods

US9828354B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9828354-B2
Application numberUS-201615272324-A
CountryUS
Kind codeB2
Filing dateSep 21, 2016
Priority dateJul 3, 2012
Publication dateNov 28, 2017
Grant dateNov 28, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The invention provides new methods for the direct umpolung self-condensation of 5-hydroxymethylfurfural (HMF) by organocatalysis, thereby upgrading the readily available substrate into 5,5′-di(hydroxymethyl) furoin (DHMF). While many efficient catalyst systems have been developed for conversion of plant biomass resources into HMF, the invention now provides methods to convert such nonfood biomass directly into DHMF by a simple process as described herein. The invention also provides highly effective new methods for upgrading other biomass furaldehydes and related compound to liquid fuels. The methods include the organocatalytic self-condensation (umpolung) of biomass furaldehydes into (C 8 -C 12 )furoin intermediates, followed by hydrogenation, etherification or esterification into oxygenated biodiesel, or hydrodeoxygenation by metal-acid tandem catalysis into premium hydrocarbon fuels.

First claim

Opening claim text (preview).

What is claimed is: 1. A compound of Formula I: wherein each R 1 is H, OH, halo, amine, alkylamino, dialkylamino, alkoxy, or acyloxy; and R 2 is OH, halo, amine, alkylamino, dialkylamino, alkoxy, or acyloxy; provided that at least one R 1 is not H. 2. The compound of claim 1 wherein each R 1 is H, OH, halo, alkoxy, or acyloxy. 3. The compound of claim 1 wherein R 2 is OH, halo, alkoxy, or acyloxy. 4. The compound of claim 1 wherein each R 1 is H, OH, halo, alkoxy, or acyloxy; and R 2 is OH, halo, alkoxy, or acyloxy. 5. The compound of claim 1 wherein the compound is: wherein each R is aryl or (C 1 -C 12 )alkyl. 6. The compound of claim 1 wherein the compound is: 7. The compound of claim 6 wherein the compound is DHMF: 8. A compound of Formula II: wherein R 1 is H, OH, halo, amine, alkylamino, dialkylamino, alkoxy, or acyloxy; and R 2 is H, OH, halo, amine, alkylamino, dialkylamino, alkoxy, or acyloxy. 9. The compound of claim 8 wherein R 1 is H, OH, halo, alkoxy, or acyloxy. 10. The compound of claim 8 wherein R 2 is H, OH, halo, alkoxy, or acyloxy. 11. The compound of claim 8 wherein R 1 is H, OH, halo, alkoxy, or acyloxy; and R 2 is H, OH, halo, alkoxy, or acyloxy. 12. The compound of claim 8 wherein the compound is: wherein each R is H, alkyl, or acyl. 13. The compound of claim 8 wherein the compound is: 14. A composition comprising a compound of claim 1 and one or more (C 8 -C 22 )alkanes. 15. The composition of claim 14 wherein the (C 8 -C 22 )alkane is a (C 10 -C 22 )alkane. 16. A composition comprising a compound of claim 7 and one or more (C 8 -C 22 )alkanes. 17. The composition of claim 16 wherein the (C 8 -C 22 )alkane is a (C 10 -C 22 )alkane. 18. A method to prepare a C 12 alkane comprising contacting a compound of Formula I: wherein each R 1 is H, OH, alkoxy, or acyloxy; and R 2 is OH, alkoxy, or acyloxy; or a compound of Formula II: wherein R 1 is H, OH, alkoxy, or acyloxy; and R 2 is H, OH, alkoxy, or acyloxy; with a bifunctional catalyst system that comprises palladium or platinum metal and an acidic moiety under reaction conditions comprising heat and H 2 pressure in water; thereby providing the C 12 alkane. 19. The method of claim 18 wherein the compound of Formula I is 5,5′-di(hydroxymethyl)furoin (DHMF), the bifunctional catalyst system is an acidic solid catalyst of the formula TaOPO 4 in combination with Pt/C, the temperature of the method is at least about 200° C., and the reaction is carried out under at least 2 MPa of hydrogen gas pressure, wherein C 12 alkane is produced. 20. The method of claim 19 wherein the temperature is at least about 300° C., and the hydrogen gas pressure is at least about 3.5 MPa.

Assignees

Inventors

Classifications

  • linked by a carbon chain containing only aliphatic carbon atoms · CPC title

  • C07D307/46Primary

    Doubly bound oxygen atoms, or two oxygen atoms singly bound to the same carbon atom · CPC title

  • Radicals substituted by oxygen atoms · CPC title

  • for compression ignition · CPC title

  • Cyclic ethers, e.g. epoxides, lactides, lactones · CPC title

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Frequently asked questions

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What does patent US9828354B2 cover?
The invention provides new methods for the direct umpolung self-condensation of 5-hydroxymethylfurfural (HMF) by organocatalysis, thereby upgrading the readily available substrate into 5,5′-di(hydroxymethyl) furoin (DHMF). While many efficient catalyst systems have been developed for conversion of plant biomass resources into HMF, the invention now provides methods to convert such nonfood bioma…
Who is the assignee on this patent?
Univ Colorado State Res Found
What technology area does this patent fall under?
Primary CPC classification C07D307/46. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Nov 28 2017 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 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).