Реакция #1605813

ord-2d5602354ea84c34b8c1ca9d286ce53d

Уравнение реакции

CC(=O)Nc1ccc(Br)cc1-c1ccccc1
2-Phenyl-4-bromo-N-acetylaniline
Cl
hydrochloric acid
Nc1ccc(Br)cc1-c1ccccc1
2-phenyl-4-bromoaniline
Выход 98.8%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe mixture was heated
  2. 2
    Температураunder reflux overnight
  3. 3
    КонцентрированиеThe solution was concentrated under reduced pressure and to the residue
  4. 4
    workup.ADDITIONwere added ethyl acetate (50 mL) and water (40 mL)
  5. 5
    Экстракцияfor extraction
  6. 6
    СушкаThe organic layer was dried over sodium sulfate
  7. 7
    Фильтрацияafter filtration
  8. 8
    Концентрированиеconcentrated under reduced pressure
  9. 9
    ДругоеThe residue was purified by a silica gel column

Методика

2-Phenyl-4-bromo-N-acetylaniline (7.79 g, 26.85 mmol) was dissolved in ethanol (100 mL), 2 N hydrochloric acid (33.56 mmol, 67.12 mL) was added dropwise under ice bath, and the mixture was heated under reflux overnight. The solution was concentrated under reduced pressure and to the residue were added ethyl acetate (50 mL) and water (40 mL) for extraction. The organic layer was dried over sodium sulfate and, after filtration, concentrated under reduced pressure. The residue was purified by a silica gel column to obtain 2-phenyl-4-bromoaniline (6.58 g).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09072734B2uspto-grants-2015_07