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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431441Generated: November 2, 2026

Sodium Carbonate → HCID 59631229, compound

https://huagongshe.com/reaction/1431441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,5-Dibromo-3-nitropyridineHCID 298470—
Reactant2-Methoxyphenylboronic acidHCID 2733958—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 59631229HCID 59631229—

Reaction Conditions

Temperature70 °C

Reaction Steps

A stirred mixture of 2,5-dibromo-3-nitropyridine (0.32 g, 1.13 mmol), 2-methoxybenzeneboronic acid (0.19 g, 1.25 mmol), tetrakis(triphenylphosphine)palladium (65.5 mg, 0.057 mmol), and 2.0M sodium carbonate (3.0 mL, 6.00 mmol) in toluene (3.0 mL) and EtOH (1.0 mL) was heated to 70° C. After 19 h, the reaction was cooled to rt then diluted with water. After extraction with EtOAc, the organic layer was dried over anhydrous sodium sulfate. After filtration and concentration, the residue was purified on silica gel (0-25% EtOAc in hexanes) to afford a light yellow solid as 5-bromo-2-(2-methoxyphenyl)-3-nitropyridine. 1H NMR (400 MHz, CDCl3) δ ppm 8.93 (1H, d, J=2.0 Hz), 8.37 (1H, d, J=2.0 Hz), 7.66 (1H, dd, J=7.5, 1.7 Hz), 7.52 (1H, m), 7.16 (1H, td, J=7.5, 1.0 Hz), 6.92 (1H, dd, J=8.3, 0.7 Hz), 3.72 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-a1c33304d11a4d6e86455103d9a81b80
Source noteuspto-grants-2015_01