HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N'-(4-chlorocyclohexyl)-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Chloro-2-methoxybenzoyl chloride | HCID 12384176 | — |
| Reactant | N-[4-(beta-acetoamido-ethyl)-benzenesulfonyl]-N'-(4-chlorocyclohexyl)-urea | HCID 21566308 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N'-(4-chlorocyclohexyl)-urea | HCID 86732946 | — |
Reaction Steps
7.8 g of N-[4-(β-acetoamido-ethyl)-benzenesulfonyl]-N'-(4-chlorocyclohexyl)-urea (melting point 151° -153°C) are heated under reflux for 2 hours with 1.6 g of sodium hydroxide and 30 ml of water. Then the whole is cooled to room temperature, 20 ml of acetone are added and 1.2 g of glacial acetic -chlorobenzamido>-ethyl)-benzenesulfonyl] acid, and 4.1 g of 2-methoxy-5-chlorobenzoylchloride are added in portions and stirring is continued for 1 hour. The precipitate if filtered off with suction, stirred with bicarbonate solution and recrystallized from methanol/dimethylformamide. The N-[4-(β-<-methoxy-5-chlorobenzamido>-ethyl)-benzenesulfonyl]-N'-(4-chlorocyclohexyl)-urea obtained melts at 178°-179°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03932503 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-3a93ce9f233441f9a4c042a988c3a7d6 |
| Source note | uspto-grants-1976_01 |