HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633947Generated: October 26, 2026
2-Aminophenol → 3-(2-Benzoxazolyl)-4-(trifluoromethoxy)benzenamine
https://huagongshe.com/reaction/1633947
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-amino-2-(trifluoromethoxy)benzoic Acid | HCID 11830994 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(2-Benzoxazolyl)-4-(trifluoromethoxy)benzenamine | HCID 22502044 | 22% |
Reaction Steps
A mixture 750 mg of 5-amino-2-trifluoromethoxybenzoic acid (750 mg, 3.39 mmol) and 2-aminophenol (370 mg, 3.39 mmol) in 10 mL of polyphosphoric acid was heated and stirred at 250° C. for 3.5 hours. The mixture was poured into ice water under stirring, followed by addition of NaHCO3 until pH 8. The mixture was extracted with ethyl acetate. The organic phase was washed with water twice, brine, rinsed with activated charcoal, dried over MgSO4 and evaporated to give an oil, which contained two compounds, according to TLC. This mixture was dissolved in DMF and separated on semi preparative HPLC (Gilson 215 Liquid Handler), stationary phase: RP18, mobile phase: Water/MeCN gradient 95%/5%-5%/95% to afford 216 mg (22%) of 3-benzoxazol-2-yl-4-trifluoromethoxyphenylamine as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06503949B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-60fde01b8bb945748e15812792aa6551 |
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| Source note | uspto-grants-2003_01 |
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