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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460455Generated: October 27, 2026

Sodium hydride → Diethyl 2-(5-chloropentyl)-2-(4,4,5,5,5-pentafluoropentyl)malonate

https://huagongshe.com/reaction/460455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-5-chloropentaneHCID 96070—
ReactantDiethyl 2-(4,4,5,5,5-pentafluoropentyl)malonateHCID 12017062—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductDiethyl 2-(5-chloropentyl)-2-(4,4,5,5,5-pentafluoropentyl)malonateHCID 2271803383%

Reaction Steps

Diethyl 2-(4,4,5,5,5-pentafluoropentyl)malonate (3 g, 9.37 mmol) was dissolved in dimethyl sulfoxide (20 ml), and sodium hydride (60%, 525 mg, 13.11 mmol) was added to the resulting solution followed by stirring for 1 hour at room temperature. 5-Bromo-1-chloropentane (7.4 ml, 56.2 mmol) was added to the reaction mixture, followed by stirring for 1.5 hours at room temperature. The reaction mixture was diluted with water, extracted with ethyl acetate, washed with water and saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate. The filtrate was concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography (eluent: dichloromethane/hexane=1/4) to give diethyl 2-(5-chloropentyl)-2-(4,4,5,5,5-pentafluoropentyl)malonate (3.3 g, Yield 83%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196081B2
Source datasetuspto-grants-2007_03
ORD IDord-bb84b16c6dea4a6c80a62702895d8f3b
Source noteuspto-grants-2007_03