Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 12529302 | HCID 12529302 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67207288 | HCID 67207288 | — |
Reaction Steps
5-ethyl-1-phenyl-1H-pyrazole (21 mg, 0.12 mmol) and N-iodosuccinimide (41 mg, 0.18 mmol) were added to acetonitrile (5 ml). The reaction mixture was heated to 60° C. After 1 hour, the reaction mixture was diluted with ethyl acetate, washed with 1N aqueous sodium hydroxide and brine, then dried over magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate/hexanes gradient) to afford 5-ethyl-4-iodo-1-phenyl-1H-pyrazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08455477B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-421b12a6bb6340fe95355bd7fa75c5f6 |
|---|
| Source note | uspto-grants-2013_06 |
|---|