HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic anhydride → 6-Chloro-1-oxo-1lambda~5~-pyridine-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Carbamide Peroxide | HCID 31294 | — |
| Reactant | 6-Chloro-3-pyridinecarbonitrile | HCID 5152094 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-Chloro-1-oxo-1lambda~5~-pyridine-3-carbonitrile | HCID 22028594 | — |
Reaction Steps
2-Chloropyridine-5-carbonitrile (7.01 g) was dissolved in acetonitrile (70 mL), and urea hydrogen peroxide addition compound (10 g) was added. Trifluoroacetic anhydride was added dropwise to the reaction mixture under ice-cooling and the mixture was stirred at room temperature for 18 hr. The reaction mixture was added to aqueous sodium thiosulfate solution and the mixture was extracted with chloroform. The extract was washed successively with saturated aqueous sodium hydrogencarbonate solution and brine and dried. The solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography to give 2-chloro-5-cyanopyridine 1-oxide (0.779 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07060722B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-6937ee50cdb24ede91596987ee8f3bea |
| Source note | uspto-grants-2006_06 |