HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → 5-[7-(4-Carbamylphenoxy)heptyl]-3-methylisoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-[7-(4-Cyanophenoxy)heptyl]-3-methylisoxazole | HCID 5271208 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-[7-(4-Carbamylphenoxy)heptyl]-3-methylisoxazole | HCID 13316962 | — |
Reaction Steps
A mixture of 4.47 g (0.015 mole) of 5-[7-(4-cyanophenoxy)heptyl]-3-methylisoxazole (Example 5), 8 ml of 30% hydrogen peroxide, 8 ml of 95% ethanol and 0.6 ml of 6 N sodium hydroxide was stirred for ten minutes. There was then added 10 ml of 95% ethanol and the reaction mixture was warmed at 40°-50° C. for 4.5 hours, then held at room temperature overnight and treated with 5% sulfuric acid to neutral pH. The mixture was cooled and the solid product collected by filtration to give 4.4 g of 5-[7-(4-carbamylphenoxy)heptyl]-3-methylisoxazole, m.p. 153°-154° C., and recrystallized from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04451476 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-834e4cc88f2b4f67ace134d6732022f0 |
| Source note | uspto-grants-1984_05 |