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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166089Generated: October 28, 2026

Ethanol → 4-(4-Methoxypyrimidin-2-YL)benzaldehyde

https://huagongshe.com/reaction/1166089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-4-methoxypyrimidineHCID 588935—
Reactant4-Formylphenylboronic AcidHCID 591073—
Catalyst(Butane-1,4-diyl)bis(diphenylphosphane)--dichloropalladium (1/1)HCID 10974057—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-(4-Methoxypyrimidin-2-YL)benzaldehydeHCID 2263105542%

Reaction Steps

1 M aq. Na2CO3 (20 mL) and ethanol (10 mL) were added to a solution of 2-chloro-4-methoxypyrimidine (2.90 g, 20.06 mmol, prepared as described in Tetrahedron 1997, 53, 11595), 4-formylphenylboronic acid (3.90 g, 26.01 mmol) and [1,4-bis(diphenylphosphino)butane]palladium(II) dichloride (0.60 g, 0.99 mmol) in toluene (40 mL) and the mixture was heated to reflux for 18 h. The cooled reaction mixture was diluted with ethyl acetate, washed with sat. aq. NaHCO3 and brine, dried (MgSO4), and concentrated. Purification by chromatography (SiO2, 4:1 hexane/ethyl acetate) yielded 1.80 g (42%) of the title compound. MS 215 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613747B2
Source datasetuspto-grants-2003_09
ORD IDord-c7839aee1f174c92b543e0ab98f05371
Source noteuspto-grants-2003_09