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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1407164Erstellt: 26. Oktober 2026

Methyl 4-methoxyacetoacetate → HCID 178496271, Verbindung

https://huagongshe.com/reaction/1407164

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 4-methoxyacetoacetateHCID 123500—
EduktSodium AcetateHCID 517045—
Edukt2,2,3,3,7-Pentafluoro-2,3-dihydro-1,4-benzodioxin-6-amineHCID 14405701—
EduktSodium NitriteHCID 23668193—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktHCID 178496271HCID 17849627185%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a suspension of 2,2,3,3,7-pentafluoro-2,3-dihydro-1,4-benzodioxin-6-amine (4.87 g, 20.2 mmol) in 6 M HCl aqueous solution (20.2 mL) was added a solution of NaNO2 (1.67 g, 24.2 mmol) in water (4 mL) at 0° C. The mixture was stirred at 0° C. for 15 min. To a suspension of methyl 4-methoxy-3-oxobutanoate (2.61 mL, 20.2 mmol) and NaOAc (30.3 g) in EtOH (34 mL) was added the above solution at 0° C. The mixture was stirred at 0° C. for 15 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 (6.84 g, 85% yield) as a red solid: 1H NMR (DMSO-d6, 300 MHz): δ ppm 3.33 (3H, s), 3.82 (3H, s), 4.68 (2H, s), 7.66-7.93 (2H, m), 12.16 (1H, brs).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08916566B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-c574079ccad545f9a49ac694fcc8463d
Quellennotizuspto-grants-2014_12