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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1805531Erstellt: 25. Oktober 2026

Methyl 4-methoxyacetoacetate → HCID 178496286, Verbindung

https://huagongshe.com/reaction/1805531

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 4-methoxyacetoacetateHCID 123500—
EduktSodium AcetateHCID 517045—
EduktSodium NitriteHCID 23668193—
Edukt2-Fluoro-5-iodoanilineHCID 25418460—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktHCID 178496286HCID 17849628687%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a suspension of 2-fluoro-5-iodoaniline (9.83 g, 41.5 mmol) in 6 M HCl aqueous solution (83.0 mL) was added a solution of NaNO2 (3.43 g, 49.8 mmol) in water (8.3 mL) at 0° C. To a suspension of methyl 4-methoxy-3-oxobutanoate (5.37 mL, 41.5 mmol) and NaOAc (124 g) in EtOH (70 mL) was added the above solution at 0° C. The mixture was stirred at 0° C. for 10 min. The precipitates were collected by filtration, washed with water, dissolved in EtOAc, washed with brine, dried over MgSO4, filtered and concentrated in vacuo to yield the title compound (14.2 g, 87% yield) as a red solid: 1H NMR (DMSO-d6, 300 MHz): δ ppm 3.31 (3H, s), 3.83 (3H, s), 4.64 (2H, s), 7.03-7.41 (1H, m), 7.43-7.66 (1H, m), 7.85-8.07 (1H, m), 12.20 (1H, brs).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08354411B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-44a57e8c78144373930310eda9d9e1d3
Quellennotizuspto-grants-2013_01