HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(1,1-Dimethylbutyl)-3-(2,5-dihydro-5-oxo-3-furyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl 4-bromo-3-oxobutanoate | HCID 295655 | — |
| Reactant | 1,1-Dimethylbutylurea | HCID 23341880 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(1,1-Dimethylbutyl)-3-(2,5-dihydro-5-oxo-3-furyl)urea | HCID 21487890 | 8% |
Reaction Steps
To a solution of 22 g of methyl-4-bromoacetoacetate in 200 ml benzene is added 14.4 g of 1,1-dimethylbutylurea and 100 mg of p-toluenesulfonic acid. The solution is heated at reflux under nitrogen for 4 hours with water removal. At the end of this period the solution is cooled and concentrated. The residual material is chromatographed on 400 g of silicic acid. Elution with a solution of benzene (60%), ethyl acetate (30%) and methanol (10%) gives crystalline material. Recrystallization of this material from ethyl acetate gives 1.8 g of 1-(1,1-dimethylbutyl)-3-(2,5-dihydro-5-oxo-3-furyl)urea, m.p. 130°-132°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03969370 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-d9640d1cef3b4732a6f9d9e67cf51a7e |
| Source note | uspto-grants-1976_07 |