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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964316Generated: November 1, 2026

Potassium Carbonate → 4-[2-(2,6-Difluorophenyl)-4,5-dihydro-4-oxazolyl]-(4-fluorophenyl)methanone

https://huagongshe.com/reaction/964316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Fluorophenylboronic acidHCID 285645—
ReactantOxazole, 2-(2,6-difluorophenyl)-4,5-dihydro-4-(4-iodophenyl)-HCID 11058111—
ReactantHCID 178418416HCID 178418416—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventAnisoleHCID 7519—
Product4-[2-(2,6-Difluorophenyl)-4,5-dihydro-4-oxazolyl]-(4-fluorophenyl)methanoneHCID 131720719276.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

The compound of Example 2 (0.5 g, 1.3 mmol) and 4-fluorophenyl boronic acid (0.27 g, 2 mmol) and potassium carbonate (fine mesh, 0.5 g, 0.4 mmol) were suspended in anisole (15 mL) and carbon monoxide was bubbled through the mixture for 5 min. Bis (triphenylphosphine) palladium chloride (0.03 g, 0.50 mmol) was added and the mixture was evacuated and carbon monoxide was released into the reaction by means of a balloon. The evacuation and carbon monoxide release was repeated and the reaction was heated to 80° C. under a carbon monoxide atmosphere for 3 h. The anisole was removed under reduced pressure and the residue was partitioned between diethylether (50 mL) and water (50 mL). The ether solution was dried over magnesium sulfate and evaporated under reduced pressure. The residue was subjected to silica gel chromatography with hexanes/ethyl acetate (5:1) as eluent to give the title compound (0.34 g) as a solid: m.p.: 105°-106° C. 1H NMR (CDCl3, 400 MHz) δ 7.9-7.0 (m,1H), 5.6 (m,1H), 4.9 (m,1H), 4.3 (m,1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767281
Source datasetuspto-grants-1998_06
ORD IDord-f16619bcf3ce43f49f45edebd89ac27f
Source noteuspto-grants-1998_06