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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 751619Erstellt: 24. Oktober 2026

Acetic Acid → Ethyl 2-bromo-5-nitro-α-oxo-4-pyridinepropanoate

https://huagongshe.com/de/reaction/751619

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktDiethyl OxalateHCID 7268—
Edukt2-Bromo-4-methyl-5-nitropyridineHCID 345873—
EduktPotassium ethoxideHCID 23670592—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktEthyl 2-bromo-5-nitro-α-oxo-4-pyridinepropanoateHCID 59753623—

Reaktionsschritte

To a solution of potassium ethoxide (2.05 g, 24.3 mmol) in diethyl ether (70 mL) and ethanol (10 mL) under an argon atmosphere was added diethyl oxalate (3.3 mL, 24.3 mmol) and the reaction stirred at rt for 15 min. A solution of 2-bromo-4-methyl-5-nitropyridine (Preparation 24, 4.8 g, 22.1 mmol) in diethyl ether (20 mL) was added to the reaction mixture giving an immediate black precipitate. The reaction was allowed to stir at rt for 6 h, then cooled to 0° C. and filtered to give a black solid. The solid was dissolved in water (250 mL) and acidified to pH 4 with acetic acid resulting in formation of a red precipitate. The solid was collected and dried to give the title compound as a red solid. δH (d6 DMSO): 1.16 (3H, t), 4.01 (2H, q), 6.55 (1H, s), 7.92 (1H, s), 8.96 (1H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07405210B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-012a2cae1fe2468fa90312d42541e3d5
Quellennotizuspto-grants-2008_07