Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | HCID 54531929 | HCID 54531929 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23452463 | HCID 23452463 | — |
Reaction Steps
20.3 g of 5-methylthio-1,3,4-thiadiazole-2-carboxylic acid cyclohexylmethylamide were dissolved in 130 ml acetic acid and 25 ml water. 16 g pulverized potassium permanganate was then introduced upon stirring to cause the temperature to increase to 70° C. Thereafter, stirring was continued for 30 minutes. The mixture was cooled and then mixed with 300 ml ice water. The formed manganese dioxide was reduced with a solution of 14.3 g sodium metabisulfite in 100 ml water. The precipitated compound was removed by suction and recrystallized from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04281121 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-910245bd2164460db4f8c359110f9c79 |
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| Source note | uspto-grants-1981_07 |
|---|