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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348156Generated: October 26, 2026

Potassium Carbonate → 4-Fluoro-2-(2-oxooxazolidin-3-yl)benzonitrile

https://huagongshe.com/reaction/348156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-4-fluorobenzonitrileHCID 118939—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant2H-1,3-oxazol-2-id-4-oneHCID 53249566—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product4-Fluoro-2-(2-oxooxazolidin-3-yl)benzonitrileHCID 2106989450%

Reaction Conditions

Temperature70 °C

Reaction Steps

A 48 mL pressure vessel containing 2-bromo-4-fluorobenzonitrile (1.00 g, 5.00 mmol), 2-oxazolidone (0.390 g, 4.50 mmol), K2CO3 (0.970 g, 7.0 mmol) and xantphos (0.231 g, 0.40 mmol) in dioxane (10 mL) was degassed with argon for 15 min. Pd2 dba3 (0.140 g, 0.15 mmol) was introduced and then the reaction mixture was heated at 70° C. for 18 h. The mixture was cooled, diluted with dioxane, and then filtered through Celite. The resulting mixture was concentrated in vacuo and subjected to column chromatography on silica gel with hexanes:ethyl acetate (1:1) to (3:7) gradient as the eluent to afford the title compound as a white solid (0.460 g, 50% yield): 1H NMR (400 MHz, CDCl3) δ ppm: 7.73 (1H, dd, J=5.8, 8.6 Hz), 7.43 (1H, dd, J=2.5, 9.6 Hz), 7.11 (1H, ddd, J=2.5, 7.5, 8.7 Hz), 4.60 (2H, t, J=7.1 Hz), 4.29 (2H, t, J=7.1 HJz); LCMS (+ESI, M+H+) m/z 207.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176196B2
Source datasetuspto-grants-2007_02
ORD IDord-1ca4e200d16d4f93acff96cbcf1e0424
Source noteuspto-grants-2007_02