Реакция #1005

ord-b9c7d82499f7455298f6c3c1fbf3995e

Уравнение реакции

O=C(O)c1c[nH]c2c1C(=O)CCC2
4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid
O=C(OOC(=O)c1ccccc1)c1ccccc1
benzoyl peroxide
O=C1CCC(=O)N1Br
N-bromosuccinimide
O=C(O)c1c(Br)[nH]c2c1C(=O)CCC2
2-bromo-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid
Выход 29.1%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe precipitate collected
  2. 2
    Промывкаrinsed with water
  3. 3
    Сушкаdiethyl ether and dried
  4. 4
    ДругоеPurification on Silica gel (5% methyl alcohol in 1:1:1 dichloromethane/ethyl acetate/hexanes)

Методика

To a solution of 4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid (886 mg, 5 mmol) and catalytic benzoyl peroxide in N,N-dimethylformamide (5 mL) at 0° C. was added N-bromosuccinimide (1.869 g, 10.5 mmol)in four equal portions over 1 hour. The mixture was stirred an additional hour, then poured into ice water, the precipitate collected and rinsed with water then diethyl ether and dried. Purification on Silica gel (5% methyl alcohol in 1:1:1 dichloromethane/ethyl acetate/hexanes) gave 2-bromo-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid (376 mg).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723462uspto-grants-1998_03