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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578594Generated: November 4, 2026

Sodium Carbonate → 4-(3-Chloropyridin-2-yl)benzaldehyde

https://huagongshe.com/reaction/578594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,3-DichloropyridineHCID 16988—
Reactant4-Formylphenylboronic AcidHCID 591073—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(3-Chloropyridin-2-yl)benzaldehydeHCID 5342623881%

Reaction Steps

{circle around (1)} 100 g (0.676 mol) of 2,3-dichloropyridine, 101.4 g (0.676 mol) of (4-formylphenyl)boronic acid and 86 g (0.811 mol) of sodium carbonate were dissolved in 500 mL of 1,2-dimethoxyethane and 500 mL of distilled water, and 78 g (0.0676 mol) of Pd(PPh3)4 was added. The mixture was heated to reflux for 18 hours so that it was allowed to react. After completion of the reaction, the reaction solution was concentrated under reduced pressure to remove 1,2-dimethoxyethane, and then extracted with ethyl acetate. The extract was treated with magnesium sulfate, filtered and concentrated under reduced pressure, yielding 4-(3-chloropyridin-2-yl)benzaldehyde as represented below in a 81% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040572B2
Source datasetuspto-grants-2015_05
ORD IDord-d521a4a5a4704322b0c7ee93df46e062
Source noteuspto-grants-2015_05