Реакция #3232

ord-b5beb2924d104c099a4a39902f3b9c14

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONto exceed 5° C. during the addition
  2. 2
    workup.ADDITIONAfter the addition
  3. 3
    Температураat reflux until the evolution of gas from the reaction mixture
  4. 4
    Температураto cool
  5. 5
    Концентрированиеwas concentrated
  6. 6
    Фильтрацияfiltered
  7. 7
    Другоеto remove the solids
  8. 8
    КонцентрированиеThe filtrate was concentrated
  9. 9
    Другоеthe residue chromatographed (eluant: diethyl ether/hexane; 1/9)

Методика

To a stirred mixture of 2-chloro-4-methyl-6-nitroaniline (7.39 g, 39.7 mM) and concentrated sulfuric acid (6.2 mL) in absolute ethanol (50 mL) at 0°-5° C. was slowly added a solution of sodium nitrite (6.85 g, 99.3 mM) in water (6 mL). The temperature of the reaction mixture was not allowed to exceed 5° C. during the addition. After the addition was completed, the reaction mixture was stirred at room temperature for 0.5 hr and then at reflux until the evolution of gas from the reaction mixture ceased. The reaction mixture was allowed to cool and was concentrated. The residue was slurried with ether and then filtered to remove the solids. The filtrate was concentrated and the residue chromatographed (eluant: diethyl ether/hexane; 1/9) to provide (6.25 g, 92%) the title compound as a yellow crystalline solid, mp 60.5-61° C.; MS(CI): 172 (M+H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05733910uspto-grants-1998_03