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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788156Generated: October 27, 2026

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

https://huagongshe.com/reaction/1788156

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 numberUS07511037B2
Source datasetuspto-grants-2009_03
ORD IDord-2aa3121b5b634996bce1262f6efb2165
Source noteuspto-grants-2009_03