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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927404Generated: October 30, 2026

Hydrochloric Acid → Diallyl 2-(4-cyanobenzyl)malonate

https://huagongshe.com/reaction/1927404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant4-(Chloromethyl)benzonitrileHCID 70127—
ReactantDiallyl malonateHCID 228227—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductDiallyl 2-(4-cyanobenzyl)malonateHCID 57831332—

Reaction Steps

19.79 g (494 mmol) of sodium hydride are added in portions (caution: evolution of hydrogen) to a solution of 121.5 g (659 mmol) of diallyl malonate in 1.5 liters of dioxane at 0° C. The mixture is warmed to room temperature and then stirred at 40° C. for 1 hour. Subsequently, at 40° C., 50 g (0.329 mol) of 4-chloromethylbenzonitrile, dissolved in 500 ml of dioxane, are slowly added dropwise, and the reaction solution is then stirred at 110° C. overnight. After cooling to room temperature, the reaction mixture is added to 1200 ml of water. Care must be taken during this that the pH is <7 (where appropriate, a few ml of 1 M hydrochloric acid are metered in to about pH 2). The mixture is then extracted three times with ethyl acetate, and the combined organic phases are washed with saturated sodium chloride solution and dried over sodium sulfate. After filtration, the solvent is concentrated to dryness in vacuo. Excess diallyl malonate is then removed by high vacuum distillation (boiling point: 57° C.; 0.074 mbar). The distillation residue is purified by flash chromatography on silica gel (mobile phase: petroleum ether/ethyl acetate 20:1). 67 g (0.22 mol, 67% of theory) of a colorless solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183271B2
Source datasetuspto-grants-2012_05
ORD IDord-26353bda82d54a8d8b5cdaaefa44652f
Source noteuspto-grants-2012_05