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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814673Generated: October 26, 2026

2-Aminophenol → 3-(2-Benzoxazolyl)-4-(trifluoromethoxy)benzenamine

https://huagongshe.com/reaction/1814673

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminophenolHCID 5801—
ReactantSodium BicarbonateHCID 516892—
Reactant5-amino-2-(trifluoromethoxy)benzoic AcidHCID 11830994—
SolventDimethylformamideHCID 6228—
Product3-(2-Benzoxazolyl)-4-(trifluoromethoxy)benzenamineHCID 2250204422%

Reaction Conditions

Temperature250 °C

Reaction Steps

A mixture 750 mg of 5-amino-2-trifluoromethoxybenzoic acid (750 mg, 3.39 mmol) and 2-aminophenol (370 mg, 3.39 mmol) in 10 mL of polyphosphoric acid was heated and stirred at 250° C. for 3.5 hours. The mixture was poured into ice water under stirring, followed by addition of NaHCO3 until pH 8. The mixture was extracted with ethyl acetate. The organic phase was washed with water twice, brine, rinsed with activated charcoal, dried over MgSO4 and evaporated to give an oil, which contained two compounds, according to TLC. This mixture was dissolved in DMF and separated on semi preparative HPLC (Gilson 215 Liquid Handler), stationary phase: RP18, mobile phase: Water/MeCN gradient 95%/5%-5%/95% to afford 216 mg (22%) of 3-benzoxazol-2-yl-4-trifluoromethoxyphenylamine as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875760B2
Source datasetuspto-grants-2005_04
ORD IDord-f1a6285e69eb43ca819565f48432c31f
Source noteuspto-grants-2005_04