HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54971Generated: October 28, 2026
Water → 2-(2-Thienylcarbonyl)benzoic acid
https://huagongshe.com/reaction/54971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | 2-(2-Thienylcarbonyl)benzoic acid | HCID 282654 | 27% |
Reaction Steps
A solution of 74.1 g (0.5 mole) of phthalic anhydride in 300 mL of nitrobenzene was treated with 147 g (1.1 mole) of aluminum chloride. The solution was stirred for two hours and 42.1 g (0.5 mole) of thiophene was added dropwise over 80 minutes at 40°-45°. The reaction was stirred at 50°-55° for two hours and then let sit at room temperature overnight. The reaction was poured into 2.8 L of cold water, stirred, separated, and the nitrobenzene was removed from the nitrobenzene layer by steam distillation. The residue was recrystallized from toluene to provide 31.1 g (27%) of 2-thienoylbenzoic acid, mp 141-143. The thienoylbenzoic acid was treated with methylhydrazine as described in Example 185 to provide 24.4 g (75%) of the phthalazinone product, mp 143-144, after recrystallization from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05624922 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-badfe0d6a3f14dbbb8f39bceae2caad5 |
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| Source note | uspto-grants-1997_04 |
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