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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267475Generated: October 31, 2026

Water → Diethyl 2-(6-heptenyl)-2-(4,4,5,5,6,6,7,7,7-nonafluoroheptyl)malonate

https://huagongshe.com/reaction/1267475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4,4,5,5,6,6,7,7,7-Nonafluoroheptyl iodideHCID 12016774—
ReactantDiethyl 2-(6-heptenyl)malonateHCID 18546274—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl 2-(6-heptenyl)-2-(4,4,5,5,6,6,7,7,7-nonafluoroheptyl)malonateHCID 12015792101.6%

Reaction Steps

60% sodium hydride (0.54 g, 13.5 mmol) was added to a solution of diethyl 2-(6-heptenyl)malonate (3.0 g, 11.7 mmol) in tetrahydrofuran (30 ml) followed by stirring for 30 minutes at room temperature. 1-Iodo-4,4,5,5,6,6,7,7,7-nonafluoroheptane (5.45 g, 14.04 mmol) was added to the mixture followed by stirring for 12 hours at room temperature. After the reaction was completed, 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 magnesium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/25) to give diethyl 2-(6-heptenyl)-2-(4,4,5,5,6,6,7,7,7-nonafluoroheptyl)malonate (6.14 g, quantitative) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552069B1
Source datasetuspto-grants-2003_04
ORD IDord-0726abbee2f64c1fbc4ef560641d4557
Source noteuspto-grants-2003_04