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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913781Generated: November 2, 2026

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

https://huagongshe.com/reaction/1913781

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 (0.494 mol) of sodium hydride are added in portions to a solution of 121.5 g (0.659 mol) of diallyl malonate in 1.5 litres of dioxane at 0° C. (caution: evolution of hydrogen). After warming to room temperature, the mixture is stirred at 40° C. for 1 hour. Subsequently, 50 g (0.329 mol) of 4-chloromethylbenzonitrile, dissolved in 500 ml of dioxane, are slowly added dropwise at 40° C., and the reaction solution is 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 remains <7 (if necessary, a few ml of 1 M hydrochloric acid are metered in until the pH is about 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 sulphate. After filtration, the solvent is evaporated 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 colourless solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609727B2
Source datasetuspto-grants-2013_12
ORD IDord-4939b6cb947a4bb2a0ca7ba06d1fb66a
Source noteuspto-grants-2013_12