Variations on prins-like chemistry to produce 2,5-dimethylhexadiene from isobutanol
View Patent ↗The method of the present invention provides a high yield pathway to 2,5-dimethylhexadiene from renewable isobutanol, which enables economic production of renewable p-xylene (and subsequently, terephthalic acid, a key monomer in the production of PET) from isobutanol. In addition, the present invention provides methods for producing 2,5-dimethylhexadiene from a variety of feed stocks that can act as “equivalents” of isobutylene and/or isobutyraldehyde including isobutanol, isobutylene oxide, and isobutyl ethers and acetals. Catalysts employed in the present methods that produce 2,5-dimethylhexadiene can also catalyze alcohol dehydration, alcohol oxidation, epoxide rearrangement, and ether and acetal cleavage.
1. A method for preparing xylenes, comprising:
a. providing a feedstock comprising isobutanol;
b. at least partially oxidizing a portion of said isobutanol to form a first stream comprising isobutyraldehyde and isobutanol;
c. coupling said isobutyraldehyde with isobutylene to form a second stream comprising 2,5-dimethyl-2,4-hexadiene; and
d. dehydrocyclizing said 2,5-dimethyl-2,4-hexadiene to form a product stream comprising said xylenes.
2. The method of claim 1 , wherein said isobutanol feedstock comprises renewable isobutanol.
3. The method of claim 2 , wherein said isobutanol feedstock is renewable isobutanol.
4. The method of claim 1 , wherein said isobutylene is formed via selective dehydration of said isobutanol in said first stream prior to said reacting step c.
5. The method of claim 1 , wherein said xylenes comprise o-xylene and p-xylene.
6. The method of claim 1 , further comprising separating said xylenes from said product stream.
7. The method of claim 1 , wherein oxidizing comprises treating said stream with an oxidizing agent.
8. The method of claim 1 , wherein said reacting step b comprises contacting said reaction mixture with a catalyst.
9. The method of claim 8 , wherein said catalyst comprises niobic acid and its hydrates.
10. The method of claim 1 , wherein the ratio of isobutyraldehyde to isobutanol in said first stream is about 1:1.
11. The method of claim 1 , further comprising conducting said coupling step c in the presence of water.
12. The method of claim 1 , further comprising conducting said coupling step c in the absence of water.
13. The method of claim 11 , further comprising conducting said coupling step in the presence of an acid.
14. The method of claim 1 , wherein said second stream further comprises one or more saturated or unsaturated mono- or polyhydroxylated octanes.
15. The method of claim 14 , wherein said one or more octanes comprise 2,5-dimethylhex-4-en-3-ol and 2,5-dimethylhexane-2,4-diol.
16. The method of claim 14 , further comprising dehydrating said one or more saturated or unsaturated mono- or polyhydroxylated octanes.
17. The method of claim 1 , wherein said oxidizing comprises dehydrogenating.