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-toluene sulfonic acid. The solution is heated at reflux under nitrogen for four 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 | US04001425 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-d2e926817b9045e19496deef48436701 |
| Source note | uspto-grants-1977_01 |