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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179996Generated: October 30, 2026

Water → 2-(2-Methoxy-4-trifluoromethoxy-phenyl)-3-methyl-5-nitro-pyridine

https://huagongshe.com/reaction/2179996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-3-methyl-5-nitropyridineHCID 89648—
Reactant(2-Methoxy-4-(trifluoromethoxy)phenyl)boronic acidHCID 22490042—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(2-Methoxy-4-trifluoromethoxy-phenyl)-3-methyl-5-nitro-pyridineHCID 22490053—

Reaction Conditions

Temperature85 °C

Reaction Steps

2-methoxy-4-trifluoromethoxybenzene boronic acid (72 g, 0.31 mol), K2CO3 (80.16 g, 0.58 mol) and water (100 ml) are added to a solution of 2-chloro-3-methyl -5-nitro-pyridine (50 g, 0.29 mol) in DME (500 ml) at room temperature. Pd(Ph3P)4 (3.35 g, 2.9 mmol) is added and the mixture is stirred at 85° C. for 19 hours. 500 ml of water is added and the mixture is extracted with EtOAc. The combined extracts are washed with brine and dried over Na2SO4. After removal of the solvent under reduced pressure, the residue is purified by flash column chromatography (hexane/EtOAc 9:1) to obtain 2-(2-methoxy-4-trifluoromethoxy-phenyl)-3-methyl-5-nitro-pyridine. Rf (hexane/EtOAc=9:1)=0.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887875B2
Source datasetuspto-grants-2005_05
ORD IDord-314049de7972427d9e1f92cd737a6b08
Source noteuspto-grants-2005_05