HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfite → 5-Benzyloxy-3-methylsulfinyl-1,2,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 5-Benzyloxy-3-methylthio-1,2,4-thiadiazole | HCID 11708511 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Benzyloxy-3-methylsulfinyl-1,2,4-thiadiazole | HCID 23032447 | — |
Reaction Steps
Into 12 ml of chloroform was dissolved 1.39 g of 5-benzyloxy-3-methylthio-1,2,4-thiadiazole, and metachloroperbenzoic acid (>70%) was slowly added to the mixture under ice-cooling. After stirring for 1 hour, the compound of low-polarity from the reaction mixture was detected by thin layer chromatography. The reaction mixture was poured into a saturated sodium sulfite aqueous solution, and separated. The organic layer was washed with sodium hydrogen carbonate aqueous solution, dried over anhydrous sodium sulfate, concentrated to give 1.4 g of 5-benzyloxy-3-methylsulfinyl-1,2,4-thiadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07273879B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-04ca18a34702406382ef4ef7c318ef5d |
| Source note | uspto-grants-2007_09 |