HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → ethyl 2,4-dimethyl-3-oxopentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl isobutyrylacetate | HCID 81583 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 2,4-dimethyl-3-oxopentanoate | HCID 225905 | 89% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of ethyl 4-methyl-3-oxopentanoate (3.0 g, 19.0 mmol) and potassium carbonate (7.86 g, 56.9 mmol) in THF (40 mL) was stirred at room temperature for 3 h under N2 (g). The mixture was cooled to 0° C. and methyl iodide (3.23 g, 22.8 mmol) was added dropwise over 5 min. The reaction mixture was allowed to warm to room temperature and stirred for 16 h. Subsequent filtration and concentration provided ethyl 2,4-dimethyl-3-oxopentanoate (2.89 g, 89% yield) as a clear yellow oil that was used without further purification. MS (EI) for C9H16O3: 172 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08648066B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-53d447776bcf4e558eb92c74c4d4bbaf |
| Source note | uspto-grants-2014_02 |