HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270171Generated: October 29, 2026
Phthalic Anhydride → HCID 46939375, compound
https://huagongshe.com/reaction/270171
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | HCID 40547758 | HCID 40547758 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 46939375 | HCID 46939375 | 80% |
Reaction Steps
A mixture of 2-amino-4-(3-chlorophenyl)-thiophene-3-carboxylic acid ethyl ester (2 mmol, Example 4 & 5, Part B) and phthalic anhydride (2.2 mmol) in glacial acetic acid; (20 mL) was heated at reflux overnight. After cooling to room temperature, the acetic acid was removed in vacuo and the residue triturated with petroleum ether. The crude product was collected by filtration, suspended in acetyl chloride (5 mL), and heated to reflux for one hour. After removing the solvent in vacuo, the residue was 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 from petroleum ether afforded the desired product as a yellow solid in 80% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07449490B2 |
|---|
| Source dataset | uspto-grants-2008_11 |
|---|
| ORD ID | ord-7235fffa5f194483b15d8f32d20057a7 |
|---|
| Source note | uspto-grants-2008_11 |
|---|