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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207492Generated: November 2, 2026

p-Fluoronitrobenzene → HCID 71015356, compound

https://huagongshe.com/reaction/2207492

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantSodium hydrideHCID 24758—
Reactant2,3-DifluorophenolHCID 80879—
CatalystCuprous chlorideHCID 62652—
SolventDimethylformamideHCID 6228—
ProductHCID 71015356HCID 7101535684.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 500 mL, 4-necked round-bottom flask purged and maintained under an inert atmosphere of nitrogen, was placed a solution of sodium hydride (6.8 g, 170.00 mmol, 1.70 equiv, 60%) in N,N-dimethylformamide (200 mL). A solution of 1-fluoro-4-nitrobenzene (14.1 g, 99.93 mmol, 1.00 equiv) in N,N-dimethylformamide (50 mL) was added dropwise with stirring at 0° C. in 15 min. The resulting solution was stirred for 2 h at room temperature. CuCl (10 g, 101.01 mmol, 1.00 equiv) was added and a solution of 2,3-difluorophenol (15.6 g, 119.91 mmol, 1.20 equiv) in N,N-dimethylformamide (50 mL) was added dropwise with stirring. The resulting solution was allowed to react, with stirring, for an additional 12 h while the temperature was maintained at 100° C. in an oil bath. The resulting solution was extracted with ether and the organic layers combined. The organic layers was washed with water and brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was loaded onto a silica gel column and eluted with ethyl acetate/petroleum ether (1:8) to give 21.2 g (84%) of 1,2-difluoro-3-(4-nitrophenoxy)benzene as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376438B2
Source datasetuspto-grants-2016_06
ORD IDord-835790d1a88840079d76890b60602a1e
Source noteuspto-grants-2016_06