HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Ethyl 4-oxo-4-(4-phenoxyphenyl)but-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 54511907 | HCID 54511907 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-oxo-4-(4-phenoxyphenyl)but-2-enoate | HCID 53776537 | 73.7% |
Reaction Steps
5.36 g of 3-(4-phenoxybenzoyl)acrylic acid were dissolved in 30 ml of dimethylformamide, and then 1.36 g of potassium carbonate and 3.08 g of diethyl sulfate were added. The mixture was stirred at room temperature for 3 hours. Diethyl ether was added to the reaction mixture, which was then washed, in turn, with water, a saturated aqueous solution of sodium hydrogencarbonate and water, and dried over magnesium sulfate. The diethyl ether was removed by evaporation under reduced pressure. The residue was purified first by silica gel column chromatography, eluted with a mixture of hexane and diethyl ether, then by recrystallization from hexane to give 4.36 g of ethyl 3-(4-phenoxybenzoyl)acrylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04472316 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-ebe378ba6dbf411bb04f4fe072dfce5f |
| Source note | uspto-grants-1984_09 |