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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664161Generated: October 27, 2026

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

https://huagongshe.com/reaction/1664161

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. Pd2dba3 (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 numberUS08039458B2
Source datasetuspto-grants-2011_10
ORD IDord-e65520a045d34883a0d231b2add29f3a
Source noteuspto-grants-2011_10