HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672698Generated: October 31, 2026
Water → Diallyl 2-(4-cyanobutyl)-2-(4-methoxycarbonylbenzyl)malonate
https://huagongshe.com/reaction/1672698
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromopentanenitrile | HCID 12470645 | — |
| Reactant | Diallyl [4-(methoxycarbonyl)benzyl]malonate | HCID 57831347 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diallyl 2-(4-cyanobutyl)-2-(4-methoxycarbonylbenzyl)malonate | HCID 57864376 | 62.3% |
Reaction Steps
1.88 g (78.23 mmol) of sodium hydride are added in portions to a solution of 20 g (60.18 mmol) of diallyl 2-(4-methoxycarbonylbenzyl)malonate from Example 12A in 140 ml of DMF at 0° C. The reaction solution is then warmed to 40° C. and is stirred at this temperature for 30 min. The reaction solution is then cooled to 0° C. again and, after addition of 10.73 g (66.20 mmol) of bromovaleronitrile in 140 ml of DMF, stirred at this temperature for 30 min. The mixture is then stirred at room temperature overnight. Water is added dropwise to the reaction mixture and, after extraction three times with ethyl acetate, 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. The resulting crude product is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 9:1→4:1). 15.5 g (37.49 mmol, 62% yield) of a colorless solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998988B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-a7f9db48c0d748678a6bbdbecf88d498 |
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| Source note | uspto-grants-2011_08 |
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