HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672951Generated: October 27, 2026
Potassium Hydroxide → 4-[(2-Fluoro-4-iodophenyl)amino]thiophene-3-carboxylic acid
https://huagongshe.com/reaction/1672951
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 4-[(2-fluoro-4-iodophenyl)amino]thiophene-3-carboxylate | HCID 66617354 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 4-[(2-Fluoro-4-iodophenyl)amino]thiophene-3-carboxylic acid | HCID 66617465 | 83% |
Reaction Steps
A mixture of methyl 4-[(2-fluoro-4-iodophenyl)amino]thiophene-3-carboxylate (0.74 g, 1.96 mmol) in the solution of potassium hydroxide (0.3 g) in ethanol/water (4 ml/4 ml) was heated up to 60° C. and stirred at this temperature for 30 min. The mixture was cooled to room temperature, diluted with 4 ml of water and extracted with ether. The water layer was acidified with 1 N HCl to pH 2, the product precipitated and was filtered off, washed several times with water and dried in vacuo to afford 4-[(2-fluoro-4-iodophenyl)amino]thiophene-3-carboxylic acid (0.59 g, 83%). 1H NMR (d6-DMSO): 13.20 (s, 1H), 9.13 (s, 1H), 8.35 (d, 1H), 7.62 (dd, 1H), 7.48-7.38 (m, 2H), 7.11 (s, 1H); MS (EI) for C11H7FINO2S: 362 (MH−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07999006B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-84beb474cc0741b985fb04a83b9d8975 |
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| Source note | uspto-grants-2011_08 |
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