HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-(2-ethylsulfanylphenyl)-6-trifluoromethyl-2H-indazole | HCID 72703661 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole | HCID 72703662 | — |
Reaction Steps
607 mg of 3-chloroperoxybenzoic acid (purity of 65% or more) was added to a mixture of 407 mg of 2-(2-ethylsulfanylphenyl)-6-trifluoromethyl-2H-indazole and 5 ml of chloroform under ice cooling, and the mixture was stirred at room temperature for 4 hours. A 10% aqueous sodium thiosulfate solution was poured to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulfate, then concentrated under reduced pressure to obtain 452 mg of 2-(2-ethylsulfonylphenyl)-6-trifluoromethyl-2H-indazole (hereinafter, referred to as Compound of Present Invention 2)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09271500B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-cc81befbaacf4c5486798342eff386c2 |
| Source note | uspto-grants-2016_03 |