Reaktion #4131

ord-5f9dfecb7ead4899b6fe668fa8962cab

Reaktionsgleichung

O=[N+]([O-])c1cc(Br)ccc1N1CCc2ccccc21
1-(2-nitro-4-bromophenyl)indoline
O=C1CCC(=O)N1Br
N-bromosuccinimide
O
water
O=[N+]([O-])c1cc(Br)ccc1N1CCc2cc(Br)ccc21
product
Ausbeute 68.0%
O=[N+]([O-])c1cc(Br)ccc1N1CCc2cc(Br)ccc21
1-(2-Nitro-4-bromophenyl)-5-bromoindoline
Ausbeute 68.0%

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe solid was filtered
  2. 2
    Sonstigedried
  3. 3
    workup.DISSOLUTIONdissolved in dichloromethane (300 ml)
  4. 4
    workup.ADDITIONThe solution was added
  5. 5
    FiltrationThe precipitate was collected by filtration

Vorschrift

To a solution of 1-(2-nitro-4-bromophenyl)indoline (15 g, 0.047 moles) in dimethylformamide (150 ml) at -10° C. was added dropwise a solution of N-bromosuccinimide (9.4 g, 0.054 mole) in dimethylformamide (50 ml) over 10 minutes. The reaction mixture was stirred at 0° C. for 15 minutes. The solution was added slowly to water (1 l) with vigorous stirring. The solid was filtered, dried, and dissolved in dichloromethane (300 ml). The solution was added to boiling methanol (1 l). The precipitate was collected by filtration to give 12.7 g (68%) of product, mp 150°-152° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04723007uspto-grants-1988_02