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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460449Generated: October 27, 2026

Water → Diethyl 2-(5-hexenyl)-2-(4,4,5,5,5-pentafluoropentyl)malonate

https://huagongshe.com/reaction/460449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-1-hexeneHCID 75906—
ReactantDiethyl 2-(4,4,5,5,5-pentafluoropentyl)malonateHCID 12017062—
SolventDimethyl SulfoxideHCID 679—
ProductDiethyl 2-(5-hexenyl)-2-(4,4,5,5,5-pentafluoropentyl)malonateHCID 2271804477%

Reaction Steps

A solution of diethyl 2-(4,4,5,5,5-pentafluoropentyl)malonate (4.0 g, 12.5 mmol) in dimethyl sulfoxide (30 ml) was cooled to 10° C. To this solution, 60% sodium hydride (600 mg, 15 mmol) was added, and the resulting mixture was stirred for 1 hour at room temperature. 6-Bromo-1-hexene (2.5 ml, 18.75 mmol) was slowly added dropwise to the reaction mixture, followed by stirring for 3 hours at room temperature. Water was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/9) to give diethyl 2-(5-hexenyl)-2-(4,4,5,5,5-pentafluoropentyl)malonate (3.86 g, Yield 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196081B2
Source datasetuspto-grants-2007_03
ORD IDord-6856c55159b6453791ce1b2bfe3d750e
Source noteuspto-grants-2007_03