HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(trifluoromethyl)nicotinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 3-[(4,4,4-Trifluoro-3-oxo-1-butenyl)amino]-2-propenenitrile | HCID 73102250 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(trifluoromethyl)nicotinonitrile | HCID 2736743 | 47.2% |
Reaction Steps
To a solution of 28% sodium methoxide (290 mg, 1.5 mmol), a solution prepared by dissolving 3-[(4,4,4-trifluoro-3-oxo-1-butenyl)amino]-2-propenenitrile (a high-polar compound IIb; 190 mg, 1.0 mmol) in methanol (2 ml) was added at room temperature and then, the mixture was refluxed for 2 hours. The reaction solution was poured into water and extracted with ethyl acetate. The organic layers were combined, washed with brine, dried over magnesium sulfate and then concentrated. The resulting residue was purified by thin layer chromatography (a developing solvent: hexane/ethyl acetate=3/1) to obtain 81.0 mg (yield 47.2%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07015236B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-6c5aa1c0b881416080dcb7f41377bb50 |
| Source note | uspto-grants-2006_03 |