Reaktion #491516

ord-7d01e7b5434b4068bfdf50d126050e0c

Reaktionsgleichung

O=C(O)c1ccc(O)cc1F
2-fluoro-4-hydroxybenzoic acid
O=S(=O)(O)O
sulfuric acid
CO
MeOH
COC(=O)c1ccc(O)cc1F
T7.1
Ausbeute 85.0%
COC(=O)c1ccc(O)cc1F
Methyl 2-fluoro-4-hydroxybenzoate
Ausbeute 85.0%

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe solvent was removed
  2. 2
    workup.ADDITIONthe residue was diluted with diethyl ether
  3. 3
    WaschenThe organic phase was washed carefully two times with saturated aqueous NaHCO3
  4. 4
    Trocknenonce with brine, and then dried over anhydrous sodium sulfate
  5. 5
    FiltrationAfter filtration
  6. 6
    Sonstigethe organic solvent was removed in vacuo

Vorschrift

To a round bottom containing 2-fluoro-4-hydroxybenzoic acid (Commercially available from TCI America) (5.34 g, 34.19 mmol) 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 residue 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 T7.1 as a white solid (5.82, 85% yield). 1H NMR (400 MHz, DMSO-d6) 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).

Quelle

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