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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181710Generated: November 2, 2026

Water → 3-(2-Nitrophenyl)pyridine

https://huagongshe.com/reaction/2181710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant1-Bromo-2-nitrobenzeneHCID 11341—
Reactant3-(Diethylboryl)pyridineHCID 642851—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
SolventDichloromethane methanolHCID 21226129—
Product3-(2-Nitrophenyl)pyridineHCID 515001941%

Reaction Steps

To a mixture consisting of 1-bromo-2-nitrobenzene (2.12 g, 8.7 mmol), diethyl (3-pyridyl) borane (1.47 g, 10.0 mmol), and bis (triphenylphosphine) palladium (II) chloride (913 mg, 1.3 mmol) in tetrahydrofuran (40 ml), sodium carbonate (4.24 g, 40.0 mmol) was added, and the resulting reaction mixture was heated at reflux for 4 hours. Water (40 ml) was added to the cooled reaction mixture which was then extracted with three 25 ml portions of ethyl acetate. The combined organic extracts were dried (anhydrous sodium sulfate) and concentrated in vacuo to afford a tacky residue. Flash chromatography of the entire sample (silica gel, 47-61 micron mesh; elution initially with methylene chloride and finally with methylene chloride/methanol=98:2 in volume) afforded the title compound as a viscous amber oil (713 mg, 41% yield). Subsequent eluent contained less pure product which was further purified by a similar flash chromatography, eluting with methylene chloride/methanol=99:1 in volume, thus affording an additional 488 mg (28% yield) of the purified title compound, again as a viscous amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894062B1
Source datasetuspto-grants-2005_05
ORD IDord-105acd0607da4daa858173a73c3bc48e
Source noteuspto-grants-2005_05