HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 4,4,4-Trifluoro-3-oxobutanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4,4-Trifluoro-3-oxobutanenitrile | HCID 13843540 | 109.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897762B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-b54d63847bac4927826f437bf2767c51 |
| Source note | uspto-grants-2011_03 |