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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552491Generated: October 30, 2026

Sodium Carbonate → 4-(3,5-Difluoro-phenyl)-2,6-dimethyl-pyrimidine

https://huagongshe.com/reaction/552491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
ReactantPotassium FluorideHCID 522689—
Reactant(3,5-Difluorophenyl)boronic acidHCID 2734338—
Reactant4-Bromo-2,6-dimethylpyrimidineHCID 10965245—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventWater ethylacetateHCID 22728543—
Product4-(3,5-Difluoro-phenyl)-2,6-dimethyl-pyrimidineHCID 6716446421%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 8.0 g, (43 mmol) of 4-Bromo-2,6-dimethyl-pyrimidine [CAS 354574-56-4], 8.1 g (51 mmol, 1.2 equiv.) of 3,5-Difluorophenylboronic acid, an 1.917 g (33.0 mmol, 3.3 equiv.) of KF in 80 ml of DME were added 20 ml of 2M sodium carbonate solution and the mixture was purged with Argon for 10 min. Then 2.24 g (8.6 mmol, 0.2 equiv.) of Triphenylphosphine and 0.96 g (4.3 mmol, 0.1 equiv.) of Palladium acetate were added and the mixture was stirred under Argon atmosphere for 18 h at 85° C. The reaction was allowed to cool to r.t., and worked up with ethyl acetate/water. The crude material was purified by flash chromatography on silicagel (heptane/ethyl acetate 1:1) to yield the title compound (1.96 g, 21%) as a red solid, MS (ISP): m/e=221.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951824B2
Source datasetuspto-grants-2011_05
ORD IDord-bb363a9efa514d4681daff64df07be48
Source noteuspto-grants-2011_05