Реакция #47825

ord-1046f77f00fd4ad4b67f07f851c18159

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияfiltered
  2. 2
    ДругоеThe organic layer was separated
  3. 3
    Концентрированиеconcentrated under a reduced pressure
  4. 4
    ДругоеThe resulting residue was purified by flash chromatography

Методика

1-Bromo-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl ester (60 mg, 0.18 mmol) obtained in Step 1 was dissolved in methanol (10 mL), silver nitrate (37.20 mg, 0.22 mmol) was added thereto, stirred for 3 hrs at RT, and filtered. The organic layer was separated, and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 14 mg of the titled compound (yield: 24%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07745439B2uspto-grants-2010_06