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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023274Generated: October 25, 2026

1,4-Dioxane → 3-Phenylpyridin-2-amine

https://huagongshe.com/reaction/1023274

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantPhenylboronic AcidHCID 66827—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-3-bromopyridineHCID 817700—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Product3-Phenylpyridin-2-amineHCID 276279570.9%

Reaction Conditions

Temperature150 °C

Reaction Steps

A microwave vial was charged with 2-amino-3-bromopyridine (0.5 g, 2.9 mmol), phenylboronic acid (0.52 g, 4.3 mmol), sodium bicarbonate (0.31 g, 2.9 mmol), dichlorobis(triphenylphosphine)palladium(II) (0.1 g, 0.14 mmol), dioxane (5 mL) and water (1 mL). The vial was capped, and the reaction mixture was heated at 150° C. for 10 min. The reaction mixture was then cooled, quenched with water (10 mL), and extracted twice with ethyl acetate. The combined organic phases were dried (MgSO4) and concentrated to leave a black oil. The crude product was purified by chromatography on silica gel using 10-40% ethyl acetate/hexanes as eluant to provide the title compound as a white solid (0.35 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722690B2
Source datasetuspto-grants-2014_05
ORD IDord-3ea3ffe98e0a40539ca6ee83d60086cb
Source noteuspto-grants-2014_05