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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(2-(4-Fluorophenyl)oxazol-4-yl)-2-hydroxyacetonitrileHCID 86674919—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-1-(2-(4-fluorophenyl)oxazol-4-yl)ethanolHCID 6732249558.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-eb9d9be991324421b9dd8bff48e16187
Source noteuspto-grants-2014_12