Concerted processes for forming 1,2,4-trihydroxybenzene from hydroquinone

Patent metadata

Field	Value
Publication number	US-10065977-B2
Application number	US-201615298175-A
Country	US
Kind code	B2
Filing date	Oct 19, 2016
Priority date	Oct 19, 2016
Publication date	Sep 4, 2018
Grant date	Sep 4, 2018

Abstract

Flow batteries incorporating an active material with one or more catecholate ligands can have a number of desirable operating features. Commercial syntheses of catechol produce significant quantities of hydroquinone as a byproduct, which presently has limited value in the battery industry and can represent a significant waste disposal issue at industrial production scales. Using a concerted, high-yield process, low-value hydroquinone can be transformed into high-value 1,2,4-trihydroxybenzene, which can be a desirable ligand for active materials of relevance in the flow battery industry. Methods for forming 1,2,4-trihydroxybenzene can include: oxidizing hydroquinone in a first reaction to form p-benzoquinone, converting the p-benzoquinone in a second reaction to form 1,2,4-triacetoxybenzene, deacetylating the 1,2,4-triacetoxybenzene in a third reaction to form 1,2,4-trihydroxybenzene, and isolating the 1,2,4-trihydroxybenzene after performing the first reaction, the second reaction and the third reaction consecutively.

First claim

What is claimed is the following:

1. A method of producing 1,2,4-trihydroxybenzene comprising the steps of:
(a) mixing p-benzoquinone in the presence of:
(i) at least two equivalents of acetic anhydride per equivalent of the p-benzoquinone, and
(ii) a catalytic amount of an acid selected from the group consisting of sulfuric acid, boron trifluoride diethyl etherate, perchloric acid, and trifluoromethanesulfonic acid,

under conditions sufficient to form a crude 1,2,4-triacetoxybenzene mixture comprising 1,2,4-triacetoxybenzene, acetic anhydride, acetic acid, and less than 0.5 mol % of 1,4-diacetoxybenzene relative to the initial p-benzoquinone;
(b) combining the crude 1,2,4-triacetoxybenzene mixture with an excess alcohol sufficient to neutralize excess acetic anhydride in the absence of added water and the presence of an acid catalyst, and heating the resulting reaction mixture under conditions sufficient to form 1,2,4-trihydroxybenzene; and
(c) isolating the 1,2,4-trihydroxybenzene.

2. The method of claim 1 , wherein the 1,2,4-triacetoxybenzene is isolated from the crude 1,2,4-triacetoxybenzene mixture by filtration from step (a), but is otherwise used without further purification before forming the 1,2,4-trihydroxybenzene in step (b).

3. The method of claim 1 , wherein the crude 1,2,4-triacetoxybenzene mixture contains less than 0.5 mol % of 1,2,4,5-tetraacetoxybenzene.

4. The method of claim 1 , wherein steps (a) and (b) are performed consecutively in a single reaction vessel.

5. The method of claim 1 , wherein step (a) is conducted in the presence of excess acetic anhydride and a catalytic amount of the acid.

6. The method of claim 5 , wherein the acid is sulfuric acid.

7. The method of claim 5 , wherein the p-benzoquinone is added to a mixture of acetic anhydride and the acid at a rate sufficient to maintain a temperature during step (b) between about 40° C. and about 50° C.

8. The method of claim 1 , wherein the alcohol used in step (b) is methanol.

9. The method of claim 1 , further comprising:
reacting the 1,2,4-trihydroxybenzene from step (b) with a transition metal precursor to form a coordination complex having 1,2,4-trihydroxybenzene as at least one ligand.

10. The method of claim 9 , wherein the coordination complex has a formula of
D g ML 1 L 2 L 3

wherein D is H, ammonium, an alkali metal, or any combination thereof; g ranges between 0 and 6; M is a transition metal; and L 1 , L 2 and L 3 are ligands, at least one of L 1 , L 2 and L 3 is a 1,2,4-trihydroxybenzene ligand.

11. The method of claim 10 , wherein D is ammonium, an alkali metal, or any combination thereof; g is 2; and M is Ti.

12. The method of claim 1 , wherein the 1,4-diacetoxybenzene formed in step (a) is limited to an amount up to about 0.3%.

13. The method of claim 1 , wherein the 1,4-diacetoxybenzene formed in step (a) is limited to an amount up to about 0.2%.

14. The method of claim 1 , wherein the 1,4-diacetoxybenzene formed in step (a) is limited to an amount up to about 0.15%.

15. The method of claim 1 , wherein step (a) is preceded by a step:
(d) oxidizing hydroquinone to form a crude p-benzoquinone product mixture comprising p-benzoquinone.

16. The method of claim 15 , wherein the oxidation of the hydroquinone is done in a solvent in the presence of hydrogen peroxide and a catalytic amount of a source of molecular iodine.

17. The method of claim 16 , wherein the solvent is ethyl acetate, isopropanol, an aqueous acid, or any combination thereof.

18. The method of claim 16 , wherein the solvent is an alcohol or ethyl acetate that is free from added water.

19. The method of claim 15 , wherein the crude p-benzoquinone product mixture is used without further purification as the source of the p-benzoquinone in step (a).

Assignees

• Lockheed Martin Advanced Energy Storage Llc

Inventors

• HUMBARGER Scott Thomas
• Millard Matthew

Classifications

• C07C37/0555 Primary

  being esterified hydroxy groups · CPC title

• C07C46/06 Primary

  of at least one hydroxy group on a six-membered aromatic ring · CPC title

• C07C67/04

  by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds · CPC title

• C07C2601/16

  the ring being unsaturated · CPC title

• C07C69/18

  of trihydroxylic compounds · CPC title