HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-tert-Butyl-1,3-diisopropylisourea → tert-Butyl 3-bromo-2-oxobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-tert-Butyl-1,3-diisopropylisourea | HCID 11041782 | — |
| Reactant | 3-Bromo-2-oxobutanoic acid | HCID 14471256 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl 3-bromo-2-oxobutanoate | HCID 23470149 | 47.7% |
Reaction Steps
A solution of 1.6 g (8.85 mmol) of 3-bromo-2-ketobutyric acid and 7 g (4 equivalents) of O-t-butyl-N,N'-diisopropylpseudourea in 14 ml methylene chloride is stirred overnight at room temperature. After filtration, the solution is washed with NaHCO3 and brine, dried and evaporated to an oil which is chromatographed on silica gel with benzene as eluant to give 1 g (45%) of t-butyl 3-bromo-2-ketobutyrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04166816 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-8607ab54ee58482e9023278d667b987a |
| Source note | uspto-grants-1979_09 |