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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 879499Erstellt: 25. Oktober 2026

Diethyl Oxalate → ethyl 2-(1-methyl-1H-indazol-5-yl)-2-oxoacetate

https://huagongshe.com/reaction/879499

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl OxalateHCID 7268—
Edukt5-Bromo-1-methyl-1H-indazoleHCID 22558725—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produktethyl 2-(1-methyl-1H-indazol-5-yl)-2-oxoacetateHCID 86700316—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To a solution of 5-bromo-1-methyl-1H-indazole (Aldrich, 1.06 g, 5 mmol) in THF (22 mL) at −78° C. was added n-butyllithium (2.2 mL, 2.5 M, 5.5 mmol) slowly. The mixture was stirred for 20 minutes, and the solution of diethyl oxalate (0.68 mL, 5.0 mmol) in THF (5 mL) was added over one minute period. The reaction was kept at −78° C. for 40 minutes, and was quenched with saturated ammonium chloride solution and warmed to 25° C. The mixture was extracted with ethyl acetate, and the organic phase was washed with water, brine, and dried over sodium sulfate. Concentration and purification with flash column chromatography (hexanes/EtOAc) gave ethyl 2-(1-methyl-1H-indazol-5-yl)-2-oxoacetate. LCMS-ESI+: calc'd for C12H13N2O3: 233.2 (M+H+); Found: 233.0 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08987250B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-a3ffd794a892427bb15dbb033853e75a
Quellennotizuspto-grants-2015_03