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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352784Generated: October 25, 2026

Diethyl Malonate → Diethyl 2-(2-nitro-4-(4-nitrobenzoyl)phenyl)malonate

https://huagongshe.com/reaction/2352784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantMalonate IonHCID 9084—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromo-3,4'-dinitro benzophenoneHCID 19708183—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductDiethyl 2-(2-nitro-4-(4-nitrobenzoyl)phenyl)malonateHCID 59256471—

Reaction Conditions

Temperature100 °C

Reaction Steps

NaH, 60% dispersion in mineral oil, (1.27 g, 31.7 mmol) was washed with petroleum ether then suspended in anhydrous DMSO (30 mL). Diethyl malonate (4.85 mL, 31.7 mmol) was dissolved in 8 mL of anhydrous DMSO and added dropwise to the NaH suspension. The mixture was allowed to stir for 15 min at 100° C., during which time the reaction mixture became homogeneous. (4-Bromo-3-nitro-phenyl)-(−4-nitro-phenyl)-methanone (5.15 g, 14.4 mmol) was dissolved in anhydrous DMSO (15 mL) and subsequently added via syringe to the malonate solution. The mixture was allowed to stir at 100° C. for 2 h after which the reaction was cooled to room temperature and poured into water (˜300 mL). The mixture was extracted with EtOAc (3×300 mL) and dried over anhydrous Na2SO4. The organic layers were then concentrated in vacuo affording a crude black oil. The crude oil was then flashed through a plug of silica with 30% EtOAc/Hexanes. The solution was then concentrated in vacuo yielding a pale yellow solid that contained the desired product contaminated with excess diethyl malonate. The impure solid was washed with Hexanes, filtered and dried affording diethyl [2-nitro-4-(4-nitrobenzoyl)phenyl] malonate in 75% yield (4.64 g, 10.8 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749530B2
Source datasetuspto-grants-2010_07
ORD IDord-1cfa05b649f542d39bb37d920e56096a
Source noteuspto-grants-2010_07