Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218520Generated: October 27, 2026

1,4-Dioxane → 2-Fluoro-3-(2-methoxy-4-nitrophenyl)pyridine

https://huagongshe.com/reaction/218520

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant1-Iodo-2-methoxy-4-nitrobenzeneHCID 230103—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Fluoropyridine-3-boronic acidHCID 2783270—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Product2-Fluoro-3-(2-methoxy-4-nitrophenyl)pyridineHCID 59586737—

Reaction Steps

2.00 g (7.17 mmol) of 2-iodo-5-nitroanisole, 2.02 g (14.3 mmol) of (2-fluoropyridin-3-yl)boronic acid (A. Bouillon, J.-C. Lancelot, V. Collot, P. R. Bovy, S. Rault, Tetrahedron 2002, 58, 3323-3328.), 1.81 g (21.5 mmol) of sodium hydrogen carbonate and 117 mg (0.14 mmol) of [1,1′-bis(diphenylphosphino)ferrocene]palladium dichloride are heated to 100° C. in a degassed mixture of 40 ml of dioxane and 10 ml of water for 1 h. After cooling, the mixture is diluted with water and extracted three times with ethyl acetate. The combined organic phases are dried over sodium sulfate, clarified over activated carbon and concentrated. Purification is effected by chromatography on silica gel (eluent: dichloromethane) to obtain 1.55 g (87% of theory) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198267B2
Source datasetuspto-grants-2012_06
ORD IDord-ff579b8070394bb5872f49f6b21404b3
Source noteuspto-grants-2012_06