HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenol → N,N'-Dicyclohexylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N,N'-Dicyclohexylurea | HCID 4277 | — |
Reaction Steps
The succinylated 2-azetidinone is dissolved in dioxane (10 ml). Anhydrous pyridine (1 ml) and p-nitrophenol (0.2 g) are added followed by dicyclohexylcarbodiimide (0.6 g, 2.5 mmole). Stirring is continued for 3 hours. The dicyclohexyl-urea formed is filtered and the filtrate is added to controlled pore glass (5 g) suspended in dimethylformamide (5 ml). Triethylamine (2 ml) is added and briefly shaken. After leaving it overnight, the CPG is filtered, washed with methanol, ether and air dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554746 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-b862b009dea744fda672e8dd5b5650a8 |
| Source note | uspto-grants-1996_09 |