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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070303Generated: October 25, 2026

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

https://huagongshe.com/reaction/2070303

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 numberUS08299108B2
Source datasetuspto-grants-2012_10
ORD IDord-7d128a329c344e9fa45c2d816f416480
Source noteuspto-grants-2012_10