HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842883Generated: November 1, 2026
Acetonitrile → 4,4,4-Trifluoro-3-oxobutanenitrile
https://huagongshe.com/reaction/1842883
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4,4,4-Trifluoro-3-oxobutanenitrile | HCID 13843540 | 98.5% |
Reaction Steps
To a stirred suspension of 60% NaH (33.80 g, 1.408 mol, 2 eq.) in dioxane (700 mL) was added acetonitrile (44.3 mL, 0.845 mol, 1.2 eq.) at 0° C. over a period of 30 min followed by ethyl trifluoroacetate (83.70 mL, 0.704 mol, 1.0 eq.). The reaction mixture was slowly and carefully heated to 10° C. for 3 h. The dioxane was evaporated under reduced pressure and the pH was adjusted to ˜6 with 1N HCl and the mixture extracted with ether (200 mL×4), dried (MgSO4) and the solvent evaporated under vacuum to get 4,4,4-trifluoro-3-oxobutanenitrile (95 g, crude, brown oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946204B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-436721f6ea4a4f9ebd172329330c7f44 |
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| Source note | uspto-grants-2015_02 |
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