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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13501Generated: October 26, 2026

p-Fluoronitrobenzene → Methyl 5-(4-nitrophenoxy)pyridine-3-carboxylate

https://huagongshe.com/reaction/13501

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-hydroxypyridine-3-carboxylateHCID 354317—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-(4-nitrophenoxy)pyridine-3-carboxylateHCID 22040734—

Reaction Conditions

Temperature80 °C

Reaction Steps

The mixture containing methyl-5-hydroxypyridine-3-carboxylate (1 eq), Potassium bis(trimethylsilyl)amide (1.2 eq) was stirred in N,N-dimethylformamide for 2 hours at room temperature. To this mixture was added 1-fluoro-4-nitrobenzene (1.1 eq) and Potassium carbonate (1.2 eq) and stirred at 80° C. for 16 h. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried, filtered and concentrated in vacuum to give brown solid. Purification on silica gel methyl-5-(4-nitrophenoxy)pyridine-3-carboxylate. MS: MH+=274.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728010B2
Source datasetuspto-grants-2010_06
ORD IDord-827bc1173d3441568cf390f6559fafd8
Source noteuspto-grants-2010_06