Process for producing pyridazinone compound and production intermediates thereof
US-2015376138-A1 · Dec 31, 2015 · US
US9434673B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9434673-B2 |
| Application number | US-201414277384-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 14, 2014 |
| Priority date | May 14, 2013 |
| Publication date | Sep 6, 2016 |
| Grant date | Sep 6, 2016 |
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Process for preparing a vinylidenecarboxylic acid or ester thereof, wherein a reaction gas comprising gaseous formaldehyde, molecular oxygen and an alkycarboxylic acid or ester thereof is brought into contact with a solid catalyst whose active composition comprises a vanadium-phosphorus oxide having an average oxidation state of vanadium of from +4.40 to +5.0 to give a product gas comprising the vinylidenecarboxylic acid or ester thereof.
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The invention claimed is: 1. A process for preparing a compound of formula (I), where R 1 and R 2 are each, independently of one another, H or (C 1 -C 4 )-alkyl, the process comprising contacting (i) a reaction gas comprising gaseous formaldehyde, molecular oxygen and a gaseous compound of formula (II) with (ii) a solid catalyst whose active composition comprises a vanadium-phosphorus oxide having an average oxidation state of vanadium of from greater than +4.65 to +5.0, to obtain a product gas comprising the compound of the formula (I). 2. The process according to claim 1 , wherein the reaction gas further comprises an inert diluent gas. 3. The process according to claim 1 , wherein the active composition comprises a vanadium-phosphorus oxide having an average oxidation state of vanadium of from greater than +4.69 to +5.0. 4. The process according to claim 1 , wherein the vanadium-phosphorus oxide has a phosphorus-vanadium atomic ratio of from 0.9 to 2.0. 5. The process according to claim 1 , wherein R 1 and R 2 in the compounds of the formulae (I) and (II) are H or CH 3 . 6. The process according to claim 1 , wherein the compound of the formula (I) is acrylic acid and the compound of the formula (II) is acetic acid. 7. The process according to claim 1 , wherein the reaction gas is brought into contact with the solid catalyst at a temperature from 250 to 400° C. 8. The process according to claim 1 , wherein the reaction gas comprises from 0.1 to 10% by volume of molecular oxygen. 9. The process according to claim 1 , wherein the reaction gas comprises from 0.5 to 10% by volume of formaldehyde. 10. The process according to claim 1 , wherein the reaction gas comprises from 1.5 to 20% by volume of the compound of the formula (II). 11. The process according to claim 1 , wherein the molar ratio of the compound of the formula (II) to formaldehyde is from 1 to 10. 12. The process according to claim 1 , wherein the compound of the formula (I) is obtained by fractional condensation of the product gas. 13. The process according to claim 1 , wherein the compound of the formula (I) is isolated from the product gas by absorption in an absorption medium and subsequent rectification of the loaded absorption medium. 14. The process according to claim 1 , wherein an all-active shaped catalyst body consisting of active composition is obtained by reacting a pentavalent vanadium compound with an organic, reducing solvent in the presence of a pentavalent phosphorus compound to give a catalyst precursor composition, shaping the catalyst precursor composition to give the shaped catalyst precursor bodies and treating the latter in an atmosphere comprising molecular oxygen at from 250 to 700° C. 15. The process according to claim 1 , further comprising preparing the formaldehyde (i) from a formaldehyde source selected from the group consisting of trioxane, paraformaldehyde, formalin, methylal, aqueous paraformaldehyde solution and aqueous formaldehyde solution, or (ii) by heterogeneously catalyzed partial gas-phase oxidation of methanol. 16. The process according to claim 6 , further comprising preparing the acetic acid by partial oxidation of ethanol or by homogeneously catalyzed carbonylation of methanol.
by isomerisation; by change of size of the carbon skeleton · CPC title
Acrylic acid; Methacrylic acid · CPC title
by reactions not involving formation of carboxyl groups · CPC title
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