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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098568Generated: October 30, 2026

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

https://huagongshe.com/reaction/1098568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantEthyl trifluoroacetateHCID 9794—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product4,4,4-Trifluoro-3-oxobutanenitrileHCID 13843540109.4%

Reaction Steps

A solution of ethyl trifluoroacetate (14.2 g, 0.1 mol) and anhydrous acetonitrile (5.0 g, 0.12 mol) in THF (100 mL) was added dropwise to a suspension of NaH (60%, 6.0 g, 0.15 mol) in THF (100 mL) at 80° C. The resulting mixture was heated to reflux overnight, and then cooled to RT. The reaction mixture was concentrated in vacuo and the residue was diluted with EtOAc and 10% aq HCl. The organic layer was washed with water and brine, dried (MgSO4) and concentrated in vacuo to yield crude 4,4,4-trifluoro-3-oxo-butyronitrile (15 g), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143293B2
Source datasetuspto-grants-2012_03
ORD IDord-01492667b1d148c3abb69e678177bd5c
Source noteuspto-grants-2012_03