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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252457Generated: November 1, 2026

Ethyl cyanoacetate → 2-Cyano-hex-5-enoic acid ethyl ester

https://huagongshe.com/reaction/252457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantHomoallyl bromideHCID 21241—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product2-Cyano-hex-5-enoic acid ethyl esterHCID 24973516—

Reaction Steps

To a flame dried flask charged with NaH (1.4 g, 35.46 mmol, 60% dispersion in mineral oil) and DMF (90 mL) equipped with a Firestone valve and under a stream of dry nitrogen was added, dropwise ethylcyanoacetate (3.14 mL, 29.56 mmol) over 20 min. The reaction mixture was then allowed to stir for 30 min, followed by addition of 4-bromobutene (3.0 mL, 29.56 mmol). The reaction mixture was allowed to stir overnight after which the solvent was removed by reduced pressure. The resulting crude mixture was dissolved in ethyl acetate, washed 3 times with 1N HCl solution and once with a saturated solution of brine. The organic and aqueous layers were separated and the organic layer was dried with sodium sulfate, filtered and the solvent was removed under reduced pressure to yield a residue. The residue was purified by flash chromatography using a mixture of 9:1 heptanes to ethyl acetate to yield a clear colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868022B2
Source datasetuspto-grants-2011_01
ORD IDord-0122ff853c3f42fb84cd13690f7d6972
Source noteuspto-grants-2011_01