HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1,3-dimethyl-4-nitro-1H-pyrazole-5-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 5-Chloro-1,3-dimethyl-4-nitro-1H-pyrazole | HCID 279515 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,3-dimethyl-4-nitro-1H-pyrazole-5-carbonitrile | HCID 96507 | — |
Reaction Steps
Fifty-five g of 1,3-dimethyl-4-nitro-5-chloropyrazole was dissolved in 400 ml acetonitrile and 17.45 g potassium cyanide added, followed by 0.5 g potassium iodide and 5 ml DMF. The mixture was refluxed for 22 hours, then cooled, and filtered. The filtrate was concentrated under reduced pressure, then added to stirred water. The resulting percipitate was collected, dried, and recyrstallized in isopropanol. mp, 85°-87° C. A second recrystallization again in ethanol gave the product having increased purity, mp 96°-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04666908 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-02e5eba2d86747a6ad61fc9c271d97c8 |
| Source note | uspto-grants-1987_05 |