Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586303Generated: October 27, 2026

Sodium Carbonate → 3-(2-Chloro-5-nitrophenyl)pyridine

https://huagongshe.com/reaction/586303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-1-chloro-4-nitrobenzeneHCID 2735549—
Reactant3-(1,3,2-Dioxaborinan-2-yl)pyridineHCID 4198005—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product3-(2-Chloro-5-nitrophenyl)pyridineHCID 2232953969%

Reaction Steps

A mixture of 3-bromo-4-chloronitrobenzene (5.17 g, 21.9 mmol) and pyridine-3-boronic acid 1,3-propanediol cyclic ester (4.27 g, 26.2 mmol) in ethanol (30 ml) and toluene (30 ml) together with 2 N Na2CO3 solution (13.9 ml) was degassed with a stream of nitrogen for 10 min. Tetrakis(triphenylphosphine)palladium(0) (0.3 g, 0.26 mmol) was added and the reaction was heated at reflux for over 24 h. The mixture was concentrated under reduced pressure to remove the organic solvents and water (100 ml) was added. This was extracted with ethyl acetate (200 ml) and then washed with brine (75 ml), dried (MgSO4), and concentrated under reduced pressure while dry loading onto silica. The resulting crude residue was purified by column chromatography (silica gel, 50% Et2O/CH2Cl2), to yield the title compound (3.53 g, 69%): 1H NMR (360 MHz, CDCl3) δ 7.42-7.48 (1H, m), 7.70 (1H, d, J 8.7 Hz), 7.81 (1H, dt, J 8.0, 1.8 Hz), 8.17-8.27 (2H, m), 8.68-8.77 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936608B2
Source datasetuspto-grants-2005_08
ORD IDord-5d81ba80b27c4c67a0b4b11fdd25b41e
Source noteuspto-grants-2005_08