HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 5,5,5-Trifluoro-4,4-dimethyl-3-oxopentanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methyl 3,3,3-trifluoro-2,2-dimethylpropanoate | HCID 53485768 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,5,5-Trifluoro-4,4-dimethyl-3-oxopentanenitrile | HCID 56954310 | 70% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a mixture of MeCN (13.9 mL, 264 mmol) in THF (500 mL) cooled to −78° C. was added n-BuLi (106 mL, 264 mmol). 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 (30 g, 176 mmol) dropwise. The mixture was stirred at 25° C. for 10 h. The mixture was quenched with aqueous NH4Cl (50 mL), extracted with EA (300 mL×3). The organic layer was dried over Na2SO4, filtered and concentrated to yield a crude product of a yellow oil of 5,5,5-trifluoro-4,4-dimethyl-3-oxopentanenitrile (22 g, 122.9 mmol, 70% yield): 1H NMR (400 MHz, CDCl3) δ 3.75 (s, 2H), 1.41 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09382238B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-c9e530d69b824e5face4131d9704de74 |
| Source note | uspto-grants-2016_07 |