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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430095Generated: November 2, 2026

Sodium Carbonate → 4-(3-Chloro-5-vinylpyridin-2-yl)benzaldehyde

https://huagongshe.com/reaction/1430095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Formylphenylboronic AcidHCID 591073—
Reactant2,3-Dichloro-5-ethenylpyridineHCID 57416849—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(3-Chloro-5-vinylpyridin-2-yl)benzaldehydeHCID 5782569894.7%

Reaction Steps

4.1 g of Na2CO3 (39 mmol), 2.0 g of 4-formylphenylboronic acid (13 mmol), and 0.45 g of Pd(PPh3)4 were added to 2.5 g of compound (8) (14.9 mmol) prepared in Example 5 dissolved in 50 mL of 1,2-dimethoxyethane and 50 mL of distilled water, and refluxed under heating and stirring for 18 hours. The mixture was cooled to room temperature, and concentrated about 50% under reduced pressure. The aqueous layer was extracted with ethyl acetate, the organic layer was dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was separated by column chromatography (eluting solvent: ethyl acetate/hexane=1/4) to obtain 3.0 g 4-(3-chloro-5-vinylpyridin-2-yl)benzaldehyde (yield 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940769B2
Source datasetuspto-grants-2015_01
ORD IDord-e9e04adaffb047cfb998a9f4402c8c8d
Source noteuspto-grants-2015_01