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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850951Generated: October 29, 2026

p-Fluoronitrobenzene → 1,3-Difluoro-2-(4-nitrophenoxy)benzene

https://huagongshe.com/reaction/1850951

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantSodium hydrideHCID 24758—
Reactant2,6-DifluorophenolHCID 94392—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1,3-Difluoro-2-(4-nitrophenoxy)benzeneHCID 1384368880.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 500-mL 4-necked round-bottom flask, was placed a solution of sodium hydride (4.05 g, 168.75 mmol, 1.70 equiv) in N,N-dimethylformamide (200 mL). A solution of 1-fluoro-4-nitrobenzene (14 g, 99.22 mmol, 1.00 equiv) in N,N-dimethylformamide (50 mL) was added dropwise with stirring at 0° C. over 20 min. The resulting solution was stirred for 2 hr at room temperature. Cu2Cl2 (9.83 g, 100.31 mmol, 1.01 equiv) was added and a solution of 2,6-difluorophenol (15.5 g, 119.15 mmol, 1.20 equiv) in N,N-dimethylformamide (50 mL) was added dropwise with stirring at 25° C. over 10 min. The resulting solution was stirred for 12 h at 100° C. in an oil bath, diluted with 500 mL of water and extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was placed on a silica gel column and eluted with ethyl acetate/petroleum ether (1/8) to give 20 g (80%) of 1,3-difluoro-2-(4-nitrophenoxy)benzene as brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957080B2
Source datasetuspto-grants-2015_02
ORD IDord-6a03bde329c94312ace15e9687c50f8b
Source noteuspto-grants-2015_02