HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl 4-methoxyphenyl ketone → HCID 18784184, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 18784184 | HCID 18784184 | 87% |
Reaction Steps
After adding potassium tert-butoxide to a solution of ethyl acetoacetate (25.7 g) in benzene (420 ml) while cooling on ice, 4-methoxyphenacyl bromide (24.8 g) was gradually added and the mixture was refluxed for an hour. After allowing the reaction solution to cool, it was washed with 5% sodium hydroxide and purified water, and dried with anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to give 26.2 g of ethyl 2-[2-(4-methoxyphenyl)-2-oxoethyl]-4-oxopentanoate (87.0% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06069176 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-cd529ceff3754de6a072eea152387e45 |
| Source note | uspto-grants-2000_05 |