Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269582Generated: October 27, 2026

Diethyl Ether → 3-(2-Bromophenyl)-5-chloro-2-(benzyloxy)pyridine

https://huagongshe.com/reaction/269582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Bromophenyl)boronic acidHCID 2773294—
Reactant2-(Benzyloxy)-3-bromo-5-chloropyridineHCID 22058382—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventToluene ethanolHCID 21863594—
Product3-(2-Bromophenyl)-5-chloro-2-(benzyloxy)pyridineHCID 5873099742.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

2-(Benzyloxy)-3-bromo-5-chloropyridine (150 mg, 0.5 mmol) and 2-bromophenylboronic acid (100 mg, 0.5 mmol) were dissolved in toluene/ethanol (1:1, 5 ml) under nitrogen. Potassium carbonate (550 mg, 4 mmol) was added, followed by tetrakis(triphenylphosphine)palladium(0) (58 mg, 0.05 mmol). The resulting mixture was heated at 70° C. in a Smithcreator® microwave for 10 minutes. After cooling, diethyl ether(10 ml) and water (10 ml) were added, The organic layer was washed with water, dried (MgSO4) and evaporated. The product was purified by flash chromatography (silica gel, 2% ethyl acetate:isohexane) to give the title compound as a clear oil (80 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446222B2
Source datasetuspto-grants-2008_11
ORD IDord-0619a99b59864bf8a00077c1d42ed192
Source noteuspto-grants-2008_11