Реакция #491516

ord-7d01e7b5434b4068bfdf50d126050e0c

Уравнение реакции

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
Выход 85.0%
COC(=O)c1ccc(O)cc1F
Methyl 2-fluoro-4-hydroxybenzoate
Выход 85.0%

Реагенты

Нет

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08748462B2uspto-grants-2014_06