Reacción #1952

ord-c5f292609ba64fafa75e76f067d6b75e

Ecuación de reacción

Cc1ccc(F)cn1
5-fluoro-2-picoline
Cc1ccc(F)cn1
5-Fluoro-2-picoline
CC(=O)OO
peracetic acid
OO
hydrogen peroxide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1ccc(F)c[n+]1[O-]
title compound
Rendimiento 22.0%
Cc1ccc(F)c[n+]1[O-]
5-Fluoro-2-picoline-N-oxide
Rendimiento 22.0%

Disolventes

Condiciones de reacción

Temperatura
50°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture was heated
  2. 2
    ExtracciónThe aqueous solution was continuously extracted with methylene chloride for 24 hours
  3. 3
    Extracciónthe methylene chloride extract
  4. 4
    Secadowas dried over anhydrous sodium sulfate
  5. 5
    Filtraciónfiltered
  6. 6
    Concentraciónconcentrated in vacuo

Procedimiento

To the solution of 5-fluoro-2-picoline obtained in Step 4, at 0° C., was added, with vigorous stirring, a cold solution of 40% peracetic acid (prepared by carefully adding 50 mL of 30% hydrogen peroxide solution to 150 mL of glacial acetic acid). The reaction mixture was heated at reflux temperature (50° C.) for 4 days and then poured into 600 mL of ice water. The aqueous mixture was adjusted to pH 9 by the addition of potassium carbonate and then was stirred at ambient temperature for 4 hours. The aqueous solution was continuously extracted with methylene chloride for 24 hours and the methylene chloride extract was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to afford 30.8 g (22% yield) of the title compound; MS DCI-NH3M/Z: 128 (M+H)+ base; 1H NMR (CDCl3) d 2.48 (s, 3H), 7.00 (ddd, 1H), 7.22 (dd, 1H), 8.22 (dd, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726182uspto-grants-1998_03