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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166003Generated: October 26, 2026

p-Fluoronitrobenzene → 2-(2-Nitro-5-fluorophenyl)-1-phenylethanone

https://huagongshe.com/reaction/1166003

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantBromineHCID 24408—
ReactantBenzene, [1-[(trimethylsilyl)oxy]ethenyl]-HCID 117406—
ReactantTris(dimethylamino)sulfonium difluorotrimethylsilicateHCID 9795567—
ReactantSodium BisulfiteHCID 23665763—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
Product2-(2-Nitro-5-fluorophenyl)-1-phenylethanoneHCID 13507910—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2.12 mL (20 mmol) of 4-fluoronitrobenzene and 4.12 mL (21 mmol) of [(1-phenyl-1-ethenyl)oxy]trimethylsilane in 30 mL of THF at -78° C. was added 5.502 g (20 mmol) of TASF dissolved in 6 mL of acetonitrile and 5 mL of THF. After stirring for 3 hrs at -78° C., 1.00 mL (19.50 mmol) of bromine in 5 mL of cyclohexane was added dropwise. After being stirred for 15 min at -78° C., the mixture was warmed to room temperature and stirred further for 30 min. Thirty mL of saturated sodium bisulfite was added, and the product was extracted into four 60 mL portions of ether. The organic phase was washed with saturated sodium chloride, dried, and concentrated. Chromatography on silica using 30% ether/hexanes yielded the expected product. The yield was 1.660 g (38%) of product, which was an oil. The product material was analyzed by infrared spectroscopy, nuclear magnetic resonance spectroscopy, and mass spectrometry.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04912220
Source datasetuspto-grants-1990_03
ORD IDord-8afe861fd18a46178036afae127fb15d
Source noteuspto-grants-1990_03