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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1801Erstellt: 24. Oktober 2026

Methanol → 2-Amino-5-bromo-alpha-(2-pyridyl)benzyl alcohol

https://huagongshe.com/de/reaction/1801

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktSodium borohydrideHCID 4311764—
Edukt2-Amino-5-bromophenyl-2-pyridylketoneHCID 69947412—
Produkt2-Amino-5-bromo-alpha-(2-pyridyl)benzyl alcoholHCID 12915500—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726306
Quelldatensatzuspto-grants-1998_03
ORD IDord-b73af90813ea458ca97a1404afcbed16
Quellennotizuspto-grants-1998_03