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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372558Generated: November 4, 2026

Diethyl Malonate → HCID 58778826, compound

https://huagongshe.com/reaction/1372558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant2-(Benzyloxy)-4-fluoro-1-nitrobenzeneHCID 11096908—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58778826HCID 58778826100%

Reaction Conditions

Temperature0 °C

Reaction Steps

In DMF (100 ml) was suspended sodium hydride (4.63 g, 115.7 mmol). Under cooling at 0° C. and stirring, diethyl malonate (18.5 g, 115.7 mmol) was added dropwise. After vigorous evolution of a hydrogen gas stopped, a solution of benzyl 5-fluoro-2-nitrophenyl ether (14.3 g, 57.8 mmol) in DMF (100 ml) was added to the reaction mixture at 0° C. The reaction mixture was stirred for 15 hours at room temperature. Water (500 ml) was poured and the mixture was extracted with ethyl acetate (300 ml). The extract was washed with saturated brine (200 ml), dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from hexane-ethyl acetate (3:1) eluate fractions, the title compound (22.0 g, 100%) was obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-9c940e15a9d448a3bcc0f4ddf9fa801a
Source noteuspto-grants-2007_01