HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967157Generated: October 31, 2026
Sodium Hydroxide → 2-Anilino-5-phenylthiophene-3-carboxylic acid
https://huagongshe.com/reaction/1967157
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-anilino-5-phenylthiophene-3-carboxylate | HCID 58256479 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Anilino-5-phenylthiophene-3-carboxylic acid | HCID 58256474 | — |
Reaction Steps
To a suspension of ethyl 2-anilino-5-phenylthiophene-3-carboxylate (51.7 mg, 0.160 mmol) in ethanol (3 mL) was added water (0.6 mL) and aqueous sodium hydroxide solution (2 M, 0.400 ml, 0.799 mmol). The reaction suspension was heated to 80° C. to afford a clear yellow solution; after one hour the suspension was allowed to cool to room temperature before being diluted with an aqueous hydrogen chloride solution (2 M, 1 mL), water (1.5 mL), and ethyl acetate (10 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (5 mL). The combined organic layers were combined and concentrated to afford 2-anilino-5-phenylthiophene-3-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420695B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-8f6e7ec8a746425fabfb7f9b73d02a28 |
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| Source note | uspto-grants-2013_04 |
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