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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Chloromethyl)benzonitrile | HCID 70127 | — |
| Reactant | Diallyl malonate | HCID 228227 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Diallyl 2-(4-cyanobenzyl)malonate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183271B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-26353bda82d54a8d8b5cdaaefa44652f |
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| Source note | uspto-grants-2012_05 |
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