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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39191Erstellt: 24. Oktober 2026

Diethyl methylmalonate → Diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate

https://huagongshe.com/de/reaction/39191

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl methylmalonateHCID 11857—
EduktSodium hydrideHCID 24758—
Edukt2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
LösungsmittelDimethylformamideHCID 6228—
ProduktDiethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonateHCID 5920613299%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Diethyl 2-methylmalonate (4.31 mL, 25.0 mmol) was dissolved in 25 mL of anhydrous DMF. This solution was cooled to 0° C. under an atmosphere of nitrogen. Sodium hydride (1.04 g, 26 mmol, 60% by weight in mineral oil) was slowly added to the solution. The resulting mixture was allowed to stir for 3 minutes at 0° C., and then at room temperature for 10 minutes. 2-Bromo-1-fluoro-4-nitrobenzene (5.00 g, 22.7 mmol) was quickly added and the mixture turned bright red. After stirring for 10 minutes at room temperature, the crude mixture was evaporated to dryness and then partitioned between dichloromethane and a saturated aqueous solution of sodium chloride. The layers were separated and the organic phase was washed twice with a saturated aqueous solution of sodium chloride. The organics were concentrated to yield diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate (8.4 g, 99%) as a pale yellow oil which was used without further purification. Retention time 1.86 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524767B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-36d28dae0c694402b63d442f4eef0be0
Quellennotizuspto-grants-2013_09