HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74276Generated: October 29, 2026
2-Aminophenol → HCID 67498799, compound
https://huagongshe.com/reaction/74276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 4-Fluoro-3-nitro-5-(trifluoromethyl)benzoic acid | HCID 24721083 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 67498799 | HCID 67498799 | 54% |
Reaction Steps
4-Fluoro-3-nitro-5-trifluoromethyl benzoic acid (1.00 g, 4.0 mmol), 2-aminophenol (0.47 g, 4.4 mmol), CHCl3 (20 mL), and WSC (0.83 g, 4.4 mmol) were added together and stirred at room temperature for 1 hour. Water was added, and this was extracted with chloroform/acetone (3:1). After the organic layer obtained was dried over anhydrous sodium sulfate, it was filtered and concentrated. To a dioxane (20 mL) solution of the solid obtained was added methanesulfonic acid (2.28 g, 24 mmol), and this was heated to reflux for 18 hours. After the reaction solution was cooled, water was added, and the precipitated crystals were filtered, and after being washed with water were dried to yield the title compound (0.70 g, 54% yield) as yellowish-brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829035B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0dc74182660c4a3da132fb85ca1a5fa0 |
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| Source note | uspto-grants-2014_09 |
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