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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050176Generated: November 1, 2026

Acetonitrile → 5,5,5-Trifluoro-4,4-dimethyl-3-oxopentanenitrile

https://huagongshe.com/reaction/1050176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantMethyl 3,3,3-trifluoro-2,2-dimethylpropanoateHCID 53485768—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5,5,5-Trifluoro-4,4-dimethyl-3-oxopentanenitrileHCID 5695431057%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a mixture of acetonitrile (3.22 g, 44.1 mmol) in THF (60 mL) at −78° C. was added n-BuLi (17.63 mL, 44.1 mmol, 2.5 mol/L). The mixture was stirred at −30° C. for 0.5 h. Then to the mixture was added methyl 3,3,3-trifluoro-2,2-dimethylpropanoate (5 g, 29.4 mmol) dropwise. Then the mixture was stirred for another 1 h. The mixture was quenched with saturated NH4Cl solution (50 mL), extracted with EA (100 mL×2). The organic layer was dried over Na2SO4, filtered and concentrated to yield a crude product as a yellow oil of 5,5,5-trifluoro-4,4-dimethyl-3-oxopentanenitrile (3 g, 16.75 mmol, 57.0% yield): 1H NMR (400 MHz, CD3OD) δ 3.75 (s, 2H), 1.40 (s., 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382238B2
Source datasetuspto-grants-2016_07
ORD IDord-46becf7e1889445699bbc46b49da77bf
Source noteuspto-grants-2016_07