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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11571Erstellt: 23. Oktober 2026

Acetamidomalonic acid diethyl ester → Diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate

https://huagongshe.com/de/reaction/11571

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetamidomalonic acid diethyl esterHCID 14041—
EduktBenzene, 2-(bromomethyl)-1-methoxy-3-nitro-HCID 186047—
EduktSodiumHCID 5360545—
LösungsmittelEthanolHCID 702—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktDiethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonateHCID 2197461580,8%

Reaktionsschritte

Sodium metal (1.15 g) was dissolved in absolute ethanol (500 mL), and to the resulting solution was added diethyl 2-acetylaminomalonate (9.1 g). After 15 min at room temperature, a solution of 2-methoxy-6-nitrobenzyl bromide (J. Med. Chem. 1977, 20, 190–196) (8.6 g) in tetrahydrofuran (25 mL) was added over 2 min. After 16 h stirring at room temperature the mixture was evaporated. The residue was dissolved in a mixture of ethyl acetate and water. The ethyl acetate layer was separated and washed sequentially with water and brine before drying over anhydrous sodium sulfate. Evaporation was followed by silica gel chromatography eluting initially with dichloromethane, followed by ethyl acetate, to obtain diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate (10.8 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098235B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-f049805b02c647ba9683e13a05b400db
Quellennotizuspto-grants-2006_08