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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213095Generated: October 26, 2026

2-Bromo-5-nitroanisole → 2-(2-Methoxy-4-nitrophenyl)pyridine

https://huagongshe.com/reaction/2213095

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-nitroanisoleHCID 101293—
ReactantHCID 178418723HCID 178418723—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Methoxy-4-nitrophenyl)pyridineHCID 21956526—

Reaction Steps

A solution of 2-bromo-5-nitroanisole (5.8 g, 25 mmol) in THF (50 mL) was treated with 2-pyridyl-zinc bromide (50 mL of a 0.5M solution in THF, 25 mmol) and Pd(PPh3)4 (1.44 g, 1.25 mmol). The reaction mixture was degassed by bubbling argon through the solution for min and was subsequently heated to reflux for 12 h while under an atmosphere of argon. The cooled reaction mixture was concentrated and purified by flash column chromatography on silica gel eluting with EtOAc:hexanes (1:19 to 2:3) to afford the desired 2-(2-methoxy-4-nitrophenyl)pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105533B2
Source datasetuspto-grants-2006_09
ORD IDord-90633e76986b47c095dae0ecbc32a69a
Source noteuspto-grants-2006_09