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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238956Generated: October 31, 2026

Water → 5-Chloro-4'-fluoro-2-nitrobiphenyl

https://huagongshe.com/reaction/238956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-FluoroiodobenzeneHCID 9605—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Chloro-2-nitrophenylboronic acidHCID 10214460—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product5-Chloro-4'-fluoro-2-nitrobiphenylHCID 67449745—

Reaction Conditions

Temperature60 °C

Reaction Steps

To water (2 mL) and dimethoxyethane (20 mL), 5-chloro-2-nitrophenylboronic acid (3.27 g, 16.4 mmol), 1-fluoro-4-iodobenzene (3.65 g, 16.4 mmol), tetrakis(triphenylphosphine)palladium (0.95 g, 0.82 mmol) and potassium carbonate (6.81 g, 49.3 mmol) were added, and the mixture was stirred under a nitrogen atmosphere at 60° C. for 2 hours. After the reaction, the reaction mixture was cooled to room temperature and ethyl acetate (30 mL) was added. After the organic phase was washed with water (30 mL) and saturated brine (20 mL), it was dried with sodium sulfate. The solvent was distilled off under reduced pressure to give 5-chloro-4′-fluoro-2-nitrobiphenyl as a crude product. The obtained compound was used for the subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642640B2
Source datasetuspto-grants-2014_02
ORD IDord-986e687770ec4c148b252687f7dae3f4
Source noteuspto-grants-2014_02