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 | — |
| 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 Ru(acac)3 was used instead of ruthenium chloride as a catalyst starting material. Consequently, the conversion of p-toluic acid was 95%, and the selectivity for terephthalic acid relative to p-toluic acid reacted was 76%. As the other products, carbon dioxide and 4-carboxybenzaldehyde were formed in the selectivities of 17%, and 2.2% respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760288 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-4c6f668fda3d4f239e049192922a7c21 |
| Source note | uspto-grants-1998_06 |