HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Tert-butyl-3-(3-oxo-1-cyclohexene-1-yl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | (1,1-Dimethylethyl)urea | HCID 14233 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-Tert-butyl-3-(3-oxo-1-cyclohexene-1-yl)urea | HCID 21486055 | 66.7% |
Reaction Steps
To a solution of 11.2 g of 1,3-cyclohexanedione in 250 ml of benzene is added 11.6 g tert-butylurea and 100 mg of p-toluenesulfonic acid. The solution is heated at reflux under nitrogen with water removal for three hours. At the end of this period the solution is cooled and the precipitated product removed by filtration. The precipitate is recrystallized from acetonitrile to give 14 g of 1-tert-butyl-3-(3-oxo-1-cyclohexene-1-yl)urea, m.p. 223°-225° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002767 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-8431755f137a43b69ed8b570e3c7ee3b |
| Source note | uspto-grants-1977_01 |