Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13501Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/13501

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-FluoronitrobenzeneHCID 9590—
EduktPotassium CarbonateHCID 11430—
EduktMethyl 5-hydroxypyridine-3-carboxylateHCID 354317—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 5-(4-nitrophenoxy)pyridine-3-carboxylateHCID 22040734—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728010B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-827bc1173d3441568cf390f6559fafd8
Quellennotizuspto-grants-2010_06