Реакция #1897

ord-b73af90813ea458ca97a1404afcbed16

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe solvent methanol was evaporated off under reduced pressure
  2. 2
    workup.ADDITIONThe residue was treated with an aqueous solution of hydrochloric acid
  3. 3
    Экстракцияextracted with ethyl acetate
  4. 4
    ПромывкаThe ethyl acetate layer was washed with water
  5. 5
    Сушкаdried over anhydrous magnesium sulfate
  6. 6
    Концентрированиеconcentrated under reduced pressure
  7. 7
    ДругоеThe residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=2:1)

Методика

In 100 ml of methanol was dissolved 10 g of 2-amino-5-bromophenyl-2-pyridylketone. To the solution was added 1.7 g of sodium borohydride and stirred for 30 minutes. The solvent methanol was evaporated off under reduced pressure. The residue was treated with an aqueous solution of hydrochloric acid. The decomposed residue was then neutralized with 200 ml of a sodium bicarbonate aqueous solution, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=2:1) to give 2-amino-5-bromo-α-(2-pyridyl)benzyl alcohol (9.0 g) as prisms, m.p. 104°-105° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726306uspto-grants-1998_03