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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194502Generated: October 31, 2026

Diethyl Malonate → Diethyl 2-(2-nitrobenzylidene)malonate

https://huagongshe.com/reaction/2194502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
Reactant2-NitrobenzaldehydeHCID 11101—
ReactantSodium BicarbonateHCID 516892—
SolventAcetic AnhydrideHCID 7918—
ProductDiethyl 2-(2-nitrobenzylidene)malonateHCID 23146060.1%

Reaction Steps

32.3 g (0.21 mol) of 2-nitrobenzaldehyde and 35.0 g (0.21 mol) of diethyl malonate were added to 100 mL of acetic anhydride at room temperature. 27.0 g (0.32 mol) of sodium hydrogen carbonate was added to this mixture, and the resulting mixture was allowed to react overnight at 100° C. The reaction mixture was concentrated under reduced pressure to approximately a half of the original volume, and ice water was added to this reaction mixture. The reaction mixture was extracted with ethyl acetate. The organic phase was washed with an aqueous solution of sodium hydrogen carbonate and water in this order, and was dried and concentrated under reduced pressure. The residue was purified by column chromatography (ethyl acetate:n-hexane=1:9 to 1:4), and thus 37.0 g (yield: 59%) of the title compound was obtained as light yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334236B2
Source datasetuspto-grants-2012_12
ORD IDord-f9027566b52444b29a7ce744c83be2e9
Source noteuspto-grants-2012_12