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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043349Generated: October 26, 2026

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

https://huagongshe.com/reaction/2043349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-BenzyloxyanilineHCID 92892—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Bromopyridine-2-carbaldehydeHCID 2757009—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product(3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-amineHCID 8662029380%

Reaction Conditions

Temperature40 °C

Reaction Steps

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]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586617B2
Source datasetuspto-grants-2013_11
ORD IDord-d8f9716ec6ae47d4b562a9d806cb07a0
Source noteuspto-grants-2013_11