HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfite → 3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfonylpyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfinylpyrazole | HCID 18929401 | — |
| Reactant | 3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfenylpyrazole | HCID 18929419 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfonylpyrazole | HCID 18929424 | — |
Reaction Steps
A 0.3 g quantity of 70% m-chloroperbenzoic acid was slowly added to 0.2 g of 3-(2,6-dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfenylpyrazole (compound 6) in 20 ml of anhydrous chloroform at room temperature with stirring, followed by further stirring overnight. The reaction mixture was poured into a 10% aqueous sodium sulfite solution, an organic layer was then separated off, washed with 5% aqueous sodium hydroxide solution and with brine and dried over anhydrous magnesium sulfate. The solvent was thereafter distilled off under reduced pressure, giving 0.3 g of the desired compound in the form of white crystals (quantitative crude yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05739083 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-98a0b3bab57c4faf8f1f3a06795f6f04 |
| Source note | uspto-grants-1998_04 |