HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Formylbenzoic acid → 2-[4-(4-Carboxystyryl)phenyl]benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | 2-(p-Tolyl)benzofuran | HCID 638458 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[4-(4-Carboxystyryl)phenyl]benzofuran | HCID 53953468 | — |
Reaction Steps
Proceeding in a manner similar to that described in Example 1 above, 2-(p-tolyl)benzofuran (2.08 g; 0.01 mole) was interacted with 2.25 g (0.01 mole) of the anil derivative of terephthalaldehydic acid in the presence of 6.72 g (0.06 mole) of potassium tert-butoxide in 150 ml of dimethylformamide. The resulting product was purified by sublimation to obtain 2-[4-(4-carboxystyryl)phenyl]benzofuran which melted at 348°-349°C. The wavelength of maximum excitation of this compound was 365 nm and the wavelength of maximum emission was 425 nm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03974144 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-abcb3afc9ede44cb83c03fa924d0d6e1 |
| Source note | uspto-grants-1976_08 |