HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-(2,2,2-Trifluoro-1-methoxyethyl)pyridine-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(2,2,2-Trifluoro-1-hydroxyethyl)pyridine-2-carbonitrile | HCID 59570313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2,2,2-Trifluoro-1-methoxyethyl)pyridine-2-carbonitrile | HCID 59570373 | 46.8% |
Reaction Steps
To 4 ml of dimethylformamide were added 0.4 g of 4-(2,2,2-trifluoro-1-hydroxyethyl)pyridine-2-carbonitrile, 0.33 g of potassium carbonate and 0.34 g of methyl iodide, and the mixture was stirred at room temperature for 20 hours. Thereafter, an aqueous saturated ammonium chloride solution was added to the reaction solution, the resultant solution was extracted with ethyl acetate three times, the organic layers were combined, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.2 g of 4-(2,2,2-trifluoro-1-methoxyethyl)pyridine-2-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318776B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-388a4c6435284c00bd9126b5c2a66ade |
| Source note | uspto-grants-2012_11 |