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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2043349Erstellt: 24. Oktober 2026

Acetic Acid → (3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-amine

https://huagongshe.com/de/reaction/2043349

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt3-BenzyloxyanilineHCID 92892—
EduktSodium BicarbonateHCID 516892—
Edukt6-Bromopyridine-2-carbaldehydeHCID 2757009—
EduktSodium triacetoxyborohydrideHCID 5049666—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelDichloromethaneHCID 6344—
Produkt(3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-amineHCID 8662029380%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To a solution of 3-benzyloxyaniline (0.70 g, 3.51 mmol) in 1,2-dichloroethane (10 ml) were added 6-bromo-pyridine-2-carboxaldehyde (0.65 g, 3.51 mmol), sodium triacetoxyborohydride (1.49 g, 7.03 mmol) and acetic acid (0.80 ml, 14.1 mmol). The reaction mixture was shaken at 40° C. overnight. For work-up dichloromethane (100 ml) and 1 M sodium bicarbonate solution (40 ml) were added and the mixture was shaken. The organic layer was separated, dried over magnesium sulfate and evaporated. The residue was purified using flash chromatography (heptane/ethyl acetate=3:1) to yield an orange oil (1.03 g, 80%); MS (ISP): 371.1 ([81Br M+H]+), 369.1 ([79Br M+H]+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08586617B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-d8f9716ec6ae47d4b562a9d806cb07a0
Quellennotizuspto-grants-2013_11