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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4,4-Trifluoro-3-oxobutanenitrile | HCID 13843540 | 56.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741479B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-81711de42184436ba1e2ed806ed4a1f0 |
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| Source note | uspto-grants-2010_06 |
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