HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → HCID 67073813, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Ethyl 2-amino-4-(4-chlorophenyl)thiophene-3-carboxylate | HCID 616598 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67073813 | HCID 67073813 | — |
Reaction Steps
A mixture of 2-amino-4-(4-chlorophenyl)thiophene-3-carboxylic acid ethyl ester (2 mmol, Example 9, Part B) and phthalic anhydride (2.2 mmol) in glacial acetic acid (20 mL) is heated at reflux overnight. After cooling to room temperature, the acetic acid is removed in vacuo and the residue triturated with petroleum ether. The crude product is collected by filtration, suspended in acetyl chloride (5 mL), and heated to reflux for one hour. After removing the solvent in vacuo, the residue is dissolved in ethyl acetate (30 mL), washed sequentially with 5% aqueous NaHCO3 (10 mL), water (10 mL), brine (10 mL), dried (Na2SO4), filtered, and concentrated in vacuo. Recrystallization affords the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07101905B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-7b7c96e150944a83861d0396f34ea23d |
| Source note | uspto-grants-2006_09 |