HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270174Generated: October 30, 2026
Phthalic Anhydride → HCID 67073891, compound
https://huagongshe.com/reaction/270174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | HCID 904007 | HCID 904007 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67073891 | HCID 67073891 | 74% |
Reaction Steps
A mixture of 2-amino-4-(3,4-dichlorophenyl)-thiophene-3-carboxylic acid ethyl ester (2 mmol, Example 6 & 7, 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 74% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449490B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-7215df2a3ba5454199a138f351885cf8 |
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| Source note | uspto-grants-2008_11 |
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