Реакция #161128

ord-2a92c40e07ad45bfada1cd9663177e5f

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwas heated
  2. 2
    Температураat reflux for 6 h
  3. 3
    Экстракцияextracted with ethyl acetate
  4. 4
    ПромывкаThe organic layer was washed with brine
  5. 5
    Сушкаdried over Na2SO4
  6. 6
    Концентрированиеconcentrated under reduced pressure
  7. 7
    ДругоеThe residue was purified by column chromatography on silica gel

Методика

A mixture of 1-benzenesulfonyl-5-ethyl-2,3-dihydro-1H-indole (15 g, 0.05 mol) in HBr (48%, 162 mL) was heated at reflux for 6 h. The mixture was basified with sat. NaOH solution to pH 9 and extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to give 5-ethyl-2,3-dihydro-1H-indole (2.5 g, 32%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08829204B2uspto-grants-2014_09