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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-BromopentanenitrileHCID 12470645—
ReactantDiallyl [4-(methoxycarbonyl)benzyl]malonateHCID 57831347—
SolventDimethylformamideHCID 6228—
ProductDiallyl 2-(4-cyanobutyl)-2-(4-methoxycarbonylbenzyl)malonateHCID 5786437662.3%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998988B2
Source datasetuspto-grants-2011_08
ORD IDord-a7f9db48c0d748678a6bbdbecf88d498
Source noteuspto-grants-2011_08