HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086802Generated: October 30, 2026
3-Nitrophenylboronic Acid → 3-(3-Nitrophenyl)pyridine
https://huagongshe.com/reaction/2086802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Nitrophenylboronic Acid | HCID 1677 | — |
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(3-Nitrophenyl)pyridine | HCID 12181327 | — |
Reaction Steps
To a mixture of 3-bromopyridine (2.6 ml) and tetrakis(triphenylphosphine)palladium(0) (0.93 g) in toluene (50 ml) was added 2M aqueous solution of sodium bicarbonate (27 ml) and a solution of dihydroxy(3-nitrophenyl)borane (5.0 g) in methanol (12 ml). The mixture was stirred at 80° C. for 6 hours and cooled. Then the mixture was poured into aqueous sodium bicarbonate and extracted with ethyl acetate twice. The combined organic phase was washed with aqueous sodium bicarbonate and brine, dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel (hexane-ethyl acetate (3:7)) to give 3-(3-nitrophenyl)pyridine (3.57 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06727245B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-9272dc126c7b4ee286d27f2520950303 |
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| Source note | uspto-grants-2004_04 |
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