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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271405Generated: October 31, 2026

Water → 4-Chloro-6-(4-chlorophenyl)pyrimidine

https://huagongshe.com/reaction/271405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant4,6-DichloropyrimidineHCID 70943—
Reactant4-Chlorophenylboronic acidHCID 74299—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product4-Chloro-6-(4-chlorophenyl)pyrimidineHCID 2490208958.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 4,6-dichloropyrimidine (1.49 g, 10.0 mmol), 4-chlorophenylboronic acid (1.72 g, 11.0 mmol) and tetrakis(triphenylphosphine)palladium (1.2 g, 1.0 mmol) in toluene (20 mL) at room temperature under argon was added aqueous Na2CO3 solution (2 M, 10 mL, 20 mmol). The resulting reaction mixture was stirred at 100° C. under argon for 6 h, after which time analysis by HPLC/MS indicated that the reaction was complete. After cooling the reaction mixture to room temperature, water (50 mL) was added. The resulting mixture was extracted with EtOAc (50 mL). The organic layer was washed with saturated aqueous NaCl, then dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by trituration with MeOH (15 mL) to obtain 1.31 g of the title compound as a white solid (purity was about 80% by HPLC analysis). HPLC/MS: retention time=3.65 min, [M+H]30 =225.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452892B2
Source datasetuspto-grants-2008_11
ORD IDord-5fae9e32d82046199a74abb086d9ce31
Source noteuspto-grants-2008_11