Reacción #1897
ord-b73af90813ea458ca97a1404afcbed16
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1OtroThe solvent methanol was evaporated off under reduced pressure
- 2workup.ADDITIONThe residue was treated with an aqueous solution of hydrochloric acid
- 3Extracciónextracted with ethyl acetate
- 4LavadoThe ethyl acetate layer was washed with water
- 5Secadodried over anhydrous magnesium sulfate
- 6Concentraciónconcentrated under reduced pressure
- 7OtroThe residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=2:1)
Procedimiento
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.