HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070034Generated: October 25, 2026
Hydrogen Peroxide → 4-(2-Hydroxyethyl)-3-(trifluoromethyl)aniline
https://huagongshe.com/reaction/2070034
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Trifluoromethyl-4-vinylaniline | HCID 23155172 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-Hydroxyethyl)-3-(trifluoromethyl)aniline | HCID 23155126 | 48% |
Reaction Steps
3-Trifluoromethyl-4-vinylaniline (2.47 g, 13.2 mmol) was dissolved in anhydrous tetrahydrofuran (10 mL), and borane.dimethyl sulfide complex (2.75 mL, 30.0 mmol) was dropwise added thereto under argon atmosphere. The mixture was stirred at room temperature for 4 hours, and then a sodium hydroxide aqueous solution (1 N, 5 mL) and a 30% hydrogen peroxide aqueous solution (3 mL) were added thereto. The resulting mixture was stirred at 0° C. for 1 hour. The reaction solution was concentrated, and the residue was partitioned between water and ethyl acetate. The organic layer was washed with saturated brine and concentrated under reduced pressure. The resulting product was purified by silica-gel column chromatography (n-hexane:ethyl acetate=2:1) to give 4-(2-hydroxyethyl)-3-(trifluoromethyl)aniline (1.3 g, 48%) as a light-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299252B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-3230b52f61c24c22ae98b945e933577f |
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| Source note | uspto-grants-2012_10 |
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