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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205293Generated: October 30, 2026

Sodium Carbonate → 3-(pyridin-4-yl)benzaldehyde

https://huagongshe.com/reaction/2205293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant3-BromobenzaldehydeHCID 76583—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
Catalystpalladium(II) acetateHCID 167845—
SolventPropan-2-ol--water (1/1)HCID 21889133—
Product3-(pyridin-4-yl)benzaldehydeHCID 279556367.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

Into a 2 L 3-necked round-bottom flask, purged and maintained with an inert atmosphere of nitrogen, was placed a solution of pyridin-4-ylboronic acid (30 g, 244 mmol, 1 equiv) in 2-propanol/water (800/40 mL), Na2CO3 (77.3 g, 729 mmol, 3 equiv), Pd(OAc)2 (5.46 g, 24.3 mmol, 0.1 equiv), PPh3 (12.75 g, 48.7 mmol, 0.2 equiv) and 3-bromobenzaldehyde (45 g, 243 mmol, 1 equiv). The mixture was stirred for 48 h at 80° C. in an oil bath. Then the solids were filtered out and the filtrate was concentrated under vacuum. The residue was purified by column chromatography on silica gel (eluting with 1:1 ethyl acetate/petroleum ether) to give 30 g of 3-(pyridin-4-yl)benzaldehyde as orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371285B2
Source datasetuspto-grants-2016_06
ORD IDord-7f66f8008bf34783b0ce3da21ab6e398
Source noteuspto-grants-2016_06