HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluic Acid → Carbon Dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluic Acid | HCID 7470 | — |
| Reactant | Terephthalic Acid | HCID 7489 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Product | Carbon Dioxide | HCID 280 | — |
| Product | 4-Formylbenzoic acid | HCID 12088 | — |
Reaction Steps
The reaction was conducted in the same manner as in Example 16 except that a product formed by charging 0.42 g of ruthenium chloride, 4.78 g of the deficient silicotungstate (K8 [SiW11O39 ].13H2O) obtained in Example 1 and 150 ml of water into a reactor at the same time (ruthenium concentration 1,000 ppm, a molar ratio of ruthenium to heteropoly-acid salt=1:1) was used as a catalyst. Consequently, the conversion of p-toluic acid was 75%. The selectivity for terephthalic acid relative to p-toluic acid reacted was 72%. As the other products, carbon dioxide and 4-carboxybenzaldehyde were formed in the selectivities of 27% and 1% respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760288 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-24531fe4ad134db492fe0aa46f69cb86 |
| Source note | uspto-grants-1998_06 |