HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640136Generated: October 31, 2026
Ethanol → [3-Amino-5-(trifluoromethyl)phenyl]propan-2-ol
https://huagongshe.com/reaction/1640136
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 2-[3-(2,5-dimethyl-1H-pyrrol-1-yl)-5-(trifluoromethyl)phenyl]propan-2-ol | HCID 58902263 | — |
| Solvent | Water | HCID 962 | — |
| Product | [3-Amino-5-(trifluoromethyl)phenyl]propan-2-ol | HCID 86613292 | — |
Reaction Steps
To a solution of 2-[3-(2,5-dimethyl-1H-pyrrol-1-yl)-5-(trifluoromethyl)phenyl]-propan-2-ol (2.29 g, 7.70 mmol) in EtOH (70 mL) and water (41 mL), was added hydroxylamine hydrochloride (16.1 g, 23.1 mmol) and potassium hydroxide (8.64 g, 154 mmol). The reaction mixture was heated at 110° C. for 18 h, and then allowed to cool to rt. The solvents were evaporated and the residue was dissolved in water and extracted with EtOAc (2×). The organic solutions were combined, washed with brine, dried over Na2SO4, filtered and evaporated. The residue was triturated with Et2O and the filtrate was evaporated to provide -[3-amino-5-(trifluoromethyl)phenyl]propan-2-ol (1.70 g, quant). 1H NMR (400 MHz,CDCl3) δ: 7.08 (s, 1H), 6.99 (s, 1H), 6.79 (s, 1H), and 1.56 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110687B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-d56dcec75bf04d02ba1132a1adbe0864 |
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| Source note | uspto-grants-2012_02 |
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