Reacción #1005

ord-b9c7d82499f7455298f6c3c1fbf3995e

Ecuación de reacción

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
Rendimiento 29.1%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe precipitate collected
  2. 2
    Lavadorinsed with water
  3. 3
    Secadodiethyl ether and dried
  4. 4
    OtroPurification on Silica gel (5% methyl alcohol in 1:1:1 dichloromethane/ethyl acetate/hexanes)

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723462uspto-grants-1998_03