HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 3-Methylsulfonyl-5-(2-methylcyclohexyl)-1,2,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 5-(2-Methylcyclohexyl)-3-methylthio-1,2,4-thiadiazole | HCID 58610442 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Methylsulfonyl-5-(2-methylcyclohexyl)-1,2,4-thiadiazole | HCID 69027281 | — |
Reaction Steps
500 mg of 5-(2-methylcyclohexyl)-3-methylthio-1,2,4-thiadiazole was dissolved in 6.5 ml of chloroform, 1.62 g of 3-chloroperoxybenzoic acid (content>65%) was added thereto taking for 20 minutes, and the reaction mixture was stirred for 30 minutes under ice-cooling and for 1.5 hours under room temperature. Then, the reaction mixture was added to saturated sodium hydrogensulfite aqueous solution, and separated. The organic layer was washed with sodium hydrogencarbonate aqueous solution, dried over anhydrous sodium sulfate, concentrated to give 466 mg of 3-methylsulfonyl-5-(2-methylcyclohexyl)-1,2,4-thiadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07301032B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-d6bce006443c4f34916cebb22f0cf0b6 |
| Source note | uspto-grants-2007_11 |