HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → HCID 136463822, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 135496353 | HCID 135496353 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136463822 | HCID 136463822 | — |
Reaction Steps
To a solution of (Z)-2-(5-cyano-2-hydroxybenzoyl)-3-hydroxypyridine O-t-butyloxime (0.98 g) in ethanol (20 ml) were added at 0° C. 6N NaOH (0.15 ml) and 30% aqueous solution of hydrogen peroxide (1.5 ml). The mixture was stirred for 2 hours at temperatures ranging from 50° to 60° C. The reaction mixture was cooled by aeration, which was then neutralized with a saturated aqueous solution of potassium hydrogensulfate, then the solvent was concentrated. The concentrate was subjected to extraction with chloroform and dried (anhydrous magnesium sulfate), followed by distilling off the solvent. The residue was recrystallized from chloroform to give (Z)-2-(5-carbamoyl-2-hydroxybenzoyl)-3-hydroxypyridine O-t-butyloxime (0.42 g) (Compound 71).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05716971 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-e81e6ab661f94be98b8ab86d257f9365 |
| Source note | uspto-grants-1998_02 |