Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409877Generated: October 31, 2026

Water → HCID 24901907, compound

https://huagongshe.com/reaction/2409877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2,4-DichloropyrimidineHCID 77531—
Reactant4-(Trifluoromethoxy)phenylboronic acidHCID 2734386—
SolventAcetonitrileHCID 6342—
ProductHCID 24901907HCID 2490190733.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a sealed tube was added 2,4-dichloropyrimidine (100 mg, 0.671 mmol), 4-(trifluoromethoxy)phenylboronic acid (138 mg, 0.671 mmol), tetrakis(triphenylphosphine)palladium0) (78 mg, 0.067 mmol), acetonitrile (2 mL) and 2M Na2CO3 in H2O (1.007 mL, 2.014 mmol). Argon was bubbled through the reaction mixture for 1 min. The reaction mixture was then sealed and stirred at 90° C. for 16 hrs. The reaction was cooled to rt and diluted with EtOAc (30 ml). The resulting organic solution was washed with water (30 ml) and saturated aqueous NaCl (30 ml). The organic layer was dried over MgSO4, filtered and concentrated. The resulting residue was purified using silica gel chromatography (ISCO system) eluting with a gradient of 0-40% EtOAc/Hex to give the product, 2-chloro-4-(4-(trifluoromethoxy)phenyl)pyrimidine, (62 mg, 0.226 mmol, 33.6% yield) as a white solid. Anal. Calcd. for C11H6ClF3N2O m/z 273.9, found: 275.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815909B2
Source datasetuspto-grants-2014_08
ORD IDord-8816b8dd7e79470aba55f6b0acb51fd3
Source noteuspto-grants-2014_08