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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50484Generated: October 27, 2026

Toluene → 3-(Pyrimidin-2-yl)benzaldehyde

https://huagongshe.com/reaction/50484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant2-ChloropyrimidineHCID 74404—
Reactant3-Formylphenylboronic acidHCID 2734356—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(Pyrimidin-2-yl)benzaldehydeHCID 2263081839.3%

Reaction Steps

EX-603A) To a toluene (15 mL) solution of 2-chloropyrimidine (1.00 g, 8.7 mmol) was added 3-formylphenylboronic acid (1.42 g, 9.5 mmol) and DMF (8 mL). To the resulting solution was added K2CO3 (2.63 g, 19.0 mmol) and Pd(PPh3)4 (0.52 g, 0.45 mmol). The slurry was heated to reflux under argon for 18 h. The cooled mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and evaporated to an oil. Purification by flash chromatography on silica gel eluting with 20% ethyl acetate in hexane gave 0.63 g (39%) of the desired 3-(2-pyrimidinyl)benzaldehyde product as a brown oil which solidified upon standing. MS: m/z=185.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710089B2
Source datasetuspto-grants-2004_03
ORD IDord-c106d404ca4a4ee281b794fdb8fe032b
Source noteuspto-grants-2004_03