HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → Cyclohexylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Cyclohexyl isothiocyanate | HCID 14289 | — |
| Reactant | Cyclohexylthiourea | HCID 1471603 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | Cyclohexylurea | HCID 69684 | — |
Reaction Steps
5 Grams N-[4-(β-<N'-methyl-N'-pyridyl-ureido>-ethyl)-benzenesulfonyl]-N'-cyclohexyl-thio-urea (prepared by reaction of 4-(β-<N'-methyl-N'-2-pyridyl-ureido>-ethyl)-benzenesulfonamide and cyclohexylisothiocyanate in an acetonic solution in the presence of potassium carbonate, melting point 143°-145° C. from methanol) were dissolved in 50 ml of 1N sodium hydroxide solution. 5 Milliliters of 30% H2O2 were added and the mixture was heated for 15 minutes on the steam bath. After cooling the solution was acidified. The precipitate was suction-filtered and recrystallized from ethanol/dimethylformamide. The N'-[4-(β-<N'-methyl-N'-2-pyridyl-ureido>-ethyl)-benzenesulfonyl]-N'-cyclohexyl-urea obtained melted at 167°-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04025519 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-aa773fd0d65e444f8b3edcfa99ad2b92 |
| Source note | uspto-grants-1977_05 |