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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1387273Erstellt: 26. Oktober 2026

Ethyl Acetate → 1-(4-Methoxybenzyl)-5-bromo-4-methyl-3-nitro-2-pyridone

https://huagongshe.com/reaction/1387273

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktSodium hydrideHCID 24758—
Edukt4-Methyloxybenzyl chlorideHCID 69993—
Edukt5-Bromo-2-hydroxy-4-methyl-3-nitropyridineHCID 21706517—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(4-Methoxybenzyl)-5-bromo-4-methyl-3-nitro-2-pyridoneHCID 2170647968%

Reaktionsschritte

To a stirred solution of 5-bromo-4-methyl-3-nitro-2-pyridone (0.60 g, 2.5 mmol) in DMF (15 mL) was added sodium hydride (60% suspension in oil, 0.103 g). After 30 minutes, 4-methoxybenzyl chloride (0.35 mL) was added, and the mixture was stirred overnight at rt. Ethyl acetate was added and the organic phase was washed with water, dried (Na2SO4), filtered and evaporated. Chromatography of the residue over silica gel (ethyl acetate/hexane 1/1)) gave 1-(4-methoxybenzyl)-5-bromo-4-methyl-3-nitro-2-pyridone (0.60 g, 1.7 mmol, 68%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06268365B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-a2fc566f34854035be24dc6d451663a6
Quellennotizuspto-grants-2001_07