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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402056Generated: October 27, 2026

Sodium Carbonate → 2-Chloro-4-(5-chloro-2-methoxyphenyl)pyridine

https://huagongshe.com/reaction/1402056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1,4-DioxaneHCID 31275—
Reactant4-Chloro-2-iodoanisoleHCID 2800978—
Reactant2-Chloropyridine-4-boronic acidHCID 5151595—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product2-Chloro-4-(5-chloro-2-methoxyphenyl)pyridineHCID 59436473—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-chloro-2-iodo-1-methoxybenzene (542 mg, 2.02 mmol), (2-chloropyridin-4-yl)boronic acid (400 mg, 2 mmol), and sodium carbonate (860.2 mg, 8.116 mmol) in 1,4-dioxane (8.4 mL, 110 mmol) and water (2.8 mL, 160 mmol) was sparged 5 minutes with argon. Tetrakis(triphenylphosphine)palladium(0) (139.9 mg, 0.1210 mmol) was added and the reaction vial was capped. The reaction mixture was heated at 90° C. After 3 hours, the reaction mixture was cooled to ambient temperature and poured into water. The mixture was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was taken up in methylene chloride, concentrated onto diatomaceous earth, and purified by automated flash chromatography (24 g SiO2, hexanes to 3:1 hexanes-ethyl acetate) to afford the product as a light yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907101B2
Source datasetuspto-grants-2014_12
ORD IDord-e8f26b4762ad4558b1c994ad862696bc
Source noteuspto-grants-2014_12