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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835441Generated: October 30, 2026

3-Nitrophenylboronic Acid → 2-(3-Nitrophenyl)pyrazine

https://huagongshe.com/reaction/1835441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
ReactantSodium CarbonateHCID 10340—
ReactantChloropyrazineHCID 73277—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(3-Nitrophenyl)pyrazineHCID 2350368388.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 2-chloropyrazine (1.14 g), 3-nitrophenylboronic acid (2.00 g) and tetrakis(triphenylphosphine)-palladium (346 mg) in 1,2-dimethoxyethane (30 ml) was added an aqueous solution of sodium carbonate (2M, 12 ml) followed by stirring at 80° C. for 18 hours. The mixture was diluted with dichloromethane and washed with water and brine. The organic layer was dried over magnesium sulfate and evaporated under reduced pressure. The residue was triturated with methanol and collected by filtration. The obtained product was washed with methanol and diisopropyl ether and dried to give 2-(3-nitrophenyl)pyrazine (1.78 g, 88.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770667B1
Source datasetuspto-grants-2004_08
ORD IDord-8991ca3cc60a42a7b357c59f25b7c6c9
Source noteuspto-grants-2004_08