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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant2-[3-(2,5-dimethyl-1H-pyrrol-1-yl)-5-(trifluoromethyl)phenyl]propan-2-olHCID 58902263—
SolventWaterHCID 962—
Product[3-Amino-5-(trifluoromethyl)phenyl]propan-2-olHCID 86613292—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110687B2
Source datasetuspto-grants-2012_02
ORD IDord-d56dcec75bf04d02ba1132a1adbe0864
Source noteuspto-grants-2012_02