HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1,3-Dihydro-1-oxoisobenzofuran-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Terephthalic Acid | HCID 7489 | — |
| Product | 1,3-Dihydro-1-oxoisobenzofuran-5-carboxylic acid | HCID 78517 | — |
Reaction Steps
In the method of the invention, the terephthalic acid is condensed with paraformaldehyde liberating water, which reacts with the SO3. When the reaction is complete, 5-carboxyphthalide may be isolated as follows. The reaction mixture is hydrolysed with water. The condensed product, 5-carboxyphthalide inclusive possible diphthalide impurities may then be filtered off, and the 5-carboxyphthalide may be dissolved in aqueous medium by adjusting pH to about 6.7 to 7.3, leaving possible diphthalide impurities in the solid phase The diphthalide present may be filtered off whereupon 5-carboxyphthalide may be precipitated by acidification, filtered off, washed with water and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06888009B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-33797d5b84e545db87aa310674f003b2 |
| Source note | uspto-grants-2005_05 |