Реакция #411407

ord-7f7a5872e19d461387095ee136dc3a75

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеfor 30 minutes
  2. 2
    Другоеthe reaction mixture partitioned between pentane (100 ml) and water (100 ml)
  3. 3
    ЭкстракцияThe aqueous phase was extracted with pentane (100 ml)
  4. 4
    Промывкаthe combined organic layers washed with saturated aqueous NaCl (100 ml), dried MgSO4), and
  5. 5
    Концентрированиеconcentrated
  6. 6
    Другоеto yield an off-white solid
  7. 7
    ДругоеPurification by flash chromatography (silica, 10% EtOAc-hexane)

Методика

To a solution of 6-bromo-2-naphthalenecarboxylic acid (Compound M) 3.1 g, (12.43 mmol) in ethanol (30 ml, 23.55 g, 511.0 mmol) was added 18M sulfuric acid (2 ml). The solution was Tefluxed for 30 minutes, cooled to room temperature, and the reaction mixture partitioned between pentane (100 ml) and water (100 ml). The aqueous phase was extracted with pentane (100 ml) and the combined organic layers washed with saturated aqueous NaCl (100 ml), dried MgSO4), and concentrated to yield an off-white solid. Purification by flash chromatography (silica, 10% EtOAc-hexane) afforded the title compound as a white solid. 1H NMR (CDCl3): δ 8.58 (1H, br s), 8.10 (1H, dd, J=1.7, 9 Hz), 8.06 (1H, d, J=2 Hz), 7.83 (1H, d, J=9 Hz), 7.80 (1H, d, J=9 Hz), 7.62 (1H, dd, J=2, 9 Hz).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06218128B1uspto-grants-2001_04