Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(2,3-Dichlorophenyl)ethan-1-one | HCID 91986 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12832890 | HCID 12832890 | 34.4% |
Reaction Steps
To 14 g of sodium hydride (50%) were added dropwise 21.3 g of diethyl oxalate, 0.54 ml of ethanol and then 160 ml of ether solution containing 30 g of 2,3-dichloroacetophenone with stirring under cooling with ice. The reaction was carried out under the state free from water. The reaction was continued at room temperature for 40 minutes with stirring after the dropping and further carried out for 45 minutes under reflux. The reaction mixture was poured into ice-cold water containing 17.5 g of acetic acid and after stirring the mixture was filtered. The organic layer was separated, dehydrated and concentrated. The residue was recrystallized from n-hexane to obtain 14.5 g of ethyl 4-(2,3-dichlorophenyl)-2,4-dioxobutyrate (white needles, m.p. 57°-58° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04326881 |
|---|
| Source dataset | uspto-grants-1982_04 |
|---|
| ORD ID | ord-efc0a605937e42e28324492bd234ace1 |
|---|
| Source note | uspto-grants-1982_04 |
|---|