Реакция #4442

ord-ed73af56968b4454b488f0c1be5537e4

Растворители

Условия реакции

Температура
10°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеdid not exceed 40° C
  2. 2
    Другоеthe layers separated
  3. 3
    Промывкаthe combined organic extracts were washed with brine (20 mL)
  4. 4
    Сушкаdried over magnesium sulfate
  5. 5
    Концентрированиеconcentrated

Методика

A solution of 2-benzyl-4-(4-pyridyl)thiazole (4.50 g, 0.018 mol) in chloroform (25 mL) was added dropwise to concentrated sulfuric acid (15 mL). The resulting mixture was cooled to 10° C. and fuming nitric acid (1.45 g, 0.97 mL) carefully added dropwise such that the reaction temperature did not exceed 40° C. The mixture was allowed to stir for thirty minutes, carefully neutralized with saturated sodium carbonate and the layers separated. The aqueous layer was reextracted with chloroform (2×25 mL) and the combined organic extracts were washed with brine (20 mL), dried over magnesium sulfate, and concentrated to afford a crude product (4.6 g). Several recrystallizations from hexane/ethyl acetate afforded pure 2-(p-nitrobenzyl)-4-(4-pyridyl)thiazole. mp. 140°-142° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04725606uspto-grants-1988_02