HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 3-Methylsulfonyl-5-(cyclohexyl)methyl-1,2,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 3-Methylthio-5-(cyclohexyl)methyl-1,2,4-thiadiazole | HCID 58610439 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Methylsulfonyl-5-(cyclohexyl)methyl-1,2,4-thiadiazole | HCID 69024542 | — |
Reaction Steps
1.2 g of 3-methylthio-5-(cyclohexyl)methyl-1,2,4-thiadiazole was dissolved in 20 ml of chloroform, 2.78 g of 3-chloroperoxybenzoic acid (content>65%) was added thereto, and the reaction mixture was stirred for 1 hour under ice-cooling and for 16 hours at 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 1.4 g of 3-methylsulfonyl-5-(cyclohexyl)methyl-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-59a78a59556248c28fc5abf310fb4ea5 |
| Source note | uspto-grants-2007_11 |