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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Nitrophenylboronic Acid | HCID 1677 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Chloropyrazine | HCID 73277 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(3-Nitrophenyl)pyrazine | HCID 23503683 | 88.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06770667B1 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-8991ca3cc60a42a7b357c59f25b7c6c9 |
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| Source note | uspto-grants-2004_08 |
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