Реакция #46173

ord-5588cf0282924f31b7a6d15cfc6a3e09

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияthe organic layer was extracted with ethyl acetate/ammonium chloride/saturated sodium chloride
  2. 2
    Сушкаdried over anhydrous magnesium sulfate
  3. 3
    Концентрированиеconcentrated
  4. 4
    Другоеthe resulting residue was purified by column chromatography

Методика

6-Bromomethyl-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (1.1 g, 2.96 mmol) was dissolved in N,N-dimethylformamide. Pyridine (264 μl, 3.26 mmol) and morpholine (284 μl, 3.26 mmol) were added thereto and the mixture was stirred for 2 hours. After the reaction was completed, the organic layer was extracted with ethyl acetate/ammonium chloride/saturated sodium chloride, dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography to obtain 180 mg of 6-(morpholine-4-yl methyl)-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (180 mg, yield 16.1%) as red oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07741323B2uspto-grants-2010_06