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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267477Generated: October 30, 2026

Water → HCID 18546289, compound

https://huagongshe.com/reaction/1267477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1,1,1,2,2,3,3,4,4-Nonafluoro-8-iodooctaneHCID 12015789—
ReactantDiethyl 2-(6-heptenyl)malonateHCID 18546274—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18546289HCID 1854628989%

Reaction Steps

A solution of diethyl 2-(6-heptenyl)malonate (3.83 g, 14.92 mmol) in anhydrous tetrahydrofuran (50 ml) was slowly added dropwise to a suspension of 60% sodium hydride (0.52 g, 12.94 mmol) in anhydrous tetrahydrofuran (150 ml) at 0° C., and the resulting mixture was stirred for 1 hour. The 1-iodo-5,5,6,6,7,7,8,8,8-nonafluorooctane prepared in Example 2 (4.0 g, 9.95 mmol) was dissolved in anhydrous tetrahydrofuran (50 ml) and then slowly added dropwise to the mixture, followed by stirring for 2 days at room temperature. After the reaction was completed, water was added to the reaction mixture, which was then extracted twice with ethyl acetate. The combined organic layers were washed with water and saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/30) to give diethyl 2-(6-heptenyl)-2-(5,5,6,6,7,7,8,8,8-nonafluorooctyl)malonate (4.7 g, Yield 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552069B1
Source datasetuspto-grants-2003_04
ORD IDord-54a9c27e211e44d781ad83e4d26c111c
Source noteuspto-grants-2003_04