Reaction #491548

ord-ed74fab914874c24ac4af66659839b9e

Conditions

Temperature
80°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherthe solvent was removed
  2. 2
    workup.ADDITIONthe mixture was diluted with diethyl ether
  3. 3
    WashThe organic phase was washed carefully two times with saturated
  4. 4
    Dryingaqueous NaHCO3, once with brine, and then dried over anhydrous sodium sulfate
  5. 5
    FiltrationAfter filtration
  6. 6
    Otherthe organic solvent was removed in vacuo

Procedure

To a round bottom containing 2-fluoro-4-hydroxybenzoic acid (5.34 g, 34.19 mmol) (commercially available from Matrix Scientific and TCI America) was added a cold solution of MeOH (50 mL) and sulfuric acid (2.0 mL). The mixture was heated to 80° C. and monitored with TLC. After 20.5 hours, the solvent was removed, and the mixture was diluted with diethyl ether. The organic phase was washed carefully two times with saturated. aqueous NaHCO3, once with brine, and then dried over anhydrous sodium sulfate. After filtration, the organic solvent was removed in vacuo to yield T31.1 as a white solid (5.82, 85% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 10.79 (1H, s), 7.75 (1H, t, J=8.8 Hz), 6.69 (1H, dd, J=8.6, 2.3 Hz), 6.62 (1H, dd, J=13.1, 2.2 Hz), 3.78 (3H, s).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08748462B2uspto-grants-2014_06