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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46384Generated: October 26, 2026

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

https://huagongshe.com/reaction/46384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Chloro-2-iodoanisoleHCID 2800978—
Reactant2-Chloropyridine-4-boronic acidHCID 5151595—
CatalystHCID 178419050HCID 178419050—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Chloro-4-(5-chloro-2-methoxyphenyl)pyridineHCID 59436473—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a nitrogen purged aqueous solution of sodium carbonate (2M, 14 mL) and ethylene glycol dimethyl ether (25 mL) was added 4-chloro-2-iodoanisole (2.50 g, 0.00931 mol), 2-chloropyridine-4-boronic acid (1.61 g, 0.0102 mol) and bis(triphenylphosphine)palladium (II) dichloride (327 mg, 0.00047 mol). The reaction mixture was warmed to 50° C. and stirred for 5 hours. Following LCMS analysis the reaction was warmed to 75° C. and stirred for 5 hours before cooling to room temperature. The reaction was partitioned between ethyl acetate (100 mL) and a 10% w/v aqueous solution of citric acid (50 mL). The organic layer was washed with water (50 mL), dried over anhydrous magnesium sulphate, filtered and the solvents removed in vacuo to give the crude product as an orange oil (2.95 g). The material was purified using an ISCO™ companion (120 g column, eluting with 100% heptane to 7:3 heptane/ethyl acetate). Fractions containing product were combined and concentrated in vacuo to obtain the title compound as an off white solid (1.10 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541588B2
Source datasetuspto-grants-2013_09
ORD IDord-79ae207cb7e44c648369753e2f7fe8dd
Source noteuspto-grants-2013_09