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

HRID 1814673Notes

Reaction equation

[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([O:11][C:12]([F:15])([F:14])[F:13])=[C:6]([CH:10]=1)[C:7]([OH:9])=O.[NH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1O.C([O-])(O)=O.[Na+]>CN(C=O)C>[O:9]1[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=2[N:16]=[C:7]1[C:6]1[CH:10]=[C:2]([NH2:1])[CH:3]=[CH:4][C:5]=1[O:11][C:12]([F:15])([F:14])[F:13]

Participants

Conditions

Temperature: 250 °C

Procedure

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.

Workup

stirringunder stirring
extractionThe mixture was extracted with ethyl acetate
washThe organic phase was washed with water twice
washbrine, rinsed with activated charcoal
dry with materialdried over MgSO4
customevaporated
customto give an oil, which
customseparated on semi preparative HPLC (Gilson 215 Liquid Handler), stationary phase

Sources & evidence

ORD record: ord-f1a6285e69eb43ca819565f48432c31f
Source dataset: uspto-grants-2005_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06875760B2

Reaction notes

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