HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447019Generated: October 25, 2026
3-Pyridinylboronic acid → HCID 57813735, compound
https://huagongshe.com/reaction/447019
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pyridinylboronic acid | HCID 2734378 | — |
| Reactant | 4-Bromo-2,6-dinitroaniline | HCID 3746608 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 57813735 | HCID 57813735 | — |
Reaction Steps
A stirred solution of 4-Bromo-2,6-dinitroaniline (3 g, 11.45 mmol) in 1,2-dimethoxyethane (83 ml) was purged with nitrogen for 15 min and treated with aqueous sodium hydrogen carbonate solution (1M, 22.8 ml) followed by pyridine 3-boronic acid (2.1 g, 17.17 mmol) and 1,1-bis-(diphenylphosphino)ferrocene palladium (II) chloride complex (0.94 g, 1.15 mmol). The resultant mixture was boiled under reflux in a nitrogen atmosphere for 18 h. After cooling to ambient temperature, the dark mixture was diluted with saturated aqueous sodium hydrogen carbonate solution (300 ml) and extracted with ethyl acetate (3×250 ml). This was dried (MgSO4) and the solvent removed in vacuo to give a residue which was purified by flash chromatography (silica) eluting with 30% to 100% ethyl acetate in 40-60 petroleum ether. The 2,6-Dinitro-4-pyridin-3-yl-aniline was obtained as a yellow solid (1.46 g, 49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481544B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-37e547226807464fb896a442f83eac94 |
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| Source note | uspto-grants-2013_07 |
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