HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → Butanoic acid, 2-ethyl-3-oxo-, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Product | Butanoic acid, 2-ethyl-3-oxo-, methyl ester | HCID 103534 | 56.8% |
Reaction Steps
465 g of methyl acetoacetate and then 458 g of ethyl bromide were added under nitrogen to 720 g of 30% sodium methylate solution. The reaction mixture was subsequently boiled at reflux. After distilling off the methanol the residue was poured onto ice-water. The mixture was then extracted with n-hexane and water. The organic phases were combined and dried. After evaporation of the solvent and distillation there were obtained 328 g of methyl 2-acetylbutyrate, b.p. 77°-79°/15 Torr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05466708 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-db0ebf60576b4b0cac38a0b425cd81b9 |
| Source note | uspto-grants-1995_11 |