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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18929Generated: October 25, 2026

Acetonitrile → 4,4,4-Trifluoro-3-oxobutanenitrile

https://huagongshe.com/reaction/18929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantEthyl trifluoroacetateHCID 9794—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product4,4,4-Trifluoro-3-oxobutanenitrileHCID 1384354056.7%

Reaction Steps

To a cooled (−78° C.) solution of LDA (2M, 15 g, 39 mmol) in anhydrous THF (50 mL) was added drop-wise a solution of ethyl trifluoroacetate (2.5 g, 18 mmol) and acetonitrile (1.4 g, 35 mmol) in 15 ml THF. The reaction was kept at −78° C. for 45 min, warmed up to room temperature over 1 hour period and quenched with ice water. The reaction was concentrated under vacuum, the residue extracted with ethyl ether, the pH brought to 1 with concentrated HCl, extracted with dichloromethane. The aqueous solution was extracted with ethyl ether, the combined organic layers dried over anhydrous sodium sulfate, and the solvent was removed under vacuum to afford 1.4 g of 4,4,4-trifluoro-3-oxobutanenitrile as a yellow oil, which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741479B2
Source datasetuspto-grants-2010_06
ORD IDord-81711de42184436ba1e2ed806ed4a1f0
Source noteuspto-grants-2010_06