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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828332Generated: October 26, 2026

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

https://huagongshe.com/reaction/1828332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidomalonic acid diethyl esterHCID 14041—
ReactantBenzene, 2-(bromomethyl)-1-methoxy-3-nitro-HCID 186047—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonateHCID 2197461580.8%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07057046B2
Source datasetuspto-grants-2006_06
ORD IDord-cdf686f2fa4b4b22bee718b4821bab64
Source noteuspto-grants-2006_06