Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472041Generated: October 30, 2026

Toluene → 2-(2,6-Dimethyl-phenyl)4-methyl-5-nitro-pyridine

https://huagongshe.com/reaction/472041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-4-methyl-5-nitropyridineHCID 345364—
Reactant2,6-Dimethylphenylboronic acidHCID 583322—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-(2,6-Dimethyl-phenyl)4-methyl-5-nitro-pyridineHCID 67152544—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2,6-dimethylphenylboronic acid (6.5 g, 43.5 mmol), 2-chloro-4-methyl-5-nitro-pyridine (5 g, 28.9 mmol), Pd(PPh3)4, (1.5 g, 1.5 mmol), Na2CO3 (4.6 g, 43.5 mmol), toluene (60 mL), water (20 mL), and EtOH (5 mL) is heated in a sealed tube under nitrogen at 110° C. for 18 hours. The mixture is cooled to room temperature, diluted with EtOAc (150 mL), washed with saturated solution of Na2CO3 (50 mL 3×), water (50 mL) and brine (50 mL), dried (Na2SO4), and concentrated under reduced pressure. The residue is purified by chromatography on silica gel (Hexane/EtOAc, 6:1) to afford 2-(2,6-dimethyl-phenyl)-4-methyl-5-nitro-pyridine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633193B2
Source datasetuspto-grants-2014_01
ORD IDord-8d3ca4143b844ae4a590884d8d852747
Source noteuspto-grants-2014_01