HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397395Generated: November 4, 2026
Trifluoroacetic acid → 2-Amino-1-(2-(4-fluorophenyl)oxazol-4-yl)ethanol
https://huagongshe.com/reaction/1397395
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(2-(4-Fluorophenyl)oxazol-4-yl)-2-hydroxyacetonitrile | HCID 86674919 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Amino-1-(2-(4-fluorophenyl)oxazol-4-yl)ethanol | HCID 67322495 | 58.7% |
Reaction Steps
Trifluoroacetic acid (0.35 mL, 4.60 mmol) was added dropwise to a suspension of NaBH4 (0.174 g, 4.60 mmol) in dry THF (10 mL) at 0° C., followed by addition of 2-(2-(4-fluorophenyl)oxazol-4-yl)-2-hydroxyacetonitrile (0.20 g, 0.92 mmol) also portionwise. The reaction mixture was stirred at room temperature for 8 h, and then concentrated under reduced pressure and diluted with ice-water. The mixture was acidified to pH ˜2 using 1.5N HCl at 0° C. and then heated to 50° C. for 20 min. The solution was basified with aqueous NH4OH solution and the organic product was extracted with CHCl3. The combined extracts were washed with brine and concentrated under reduced pressure to afford 2-amino-1-(2-(4-fluorophenyl)oxazol-4-yl)ethanol (120 mg, crude), which was carried through without further purification. MS (ESI) m/z: Calculated for C11H11FN2O2: 222.08. found: 222.8 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901156B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-eb9d9be991324421b9dd8bff48e16187 |
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| Source note | uspto-grants-2014_12 |
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