HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethyl 4-(3,4-dichlorophenyl)-2,4-dioxobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Ethanone, 1-(3,4-dichlorophenyl)- | HCID 75841 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 4-(3,4-dichlorophenyl)-2,4-dioxobutanoate | HCID 10017017 | — |
Reaction Steps
To a solution of t-BuOK (0.05 mol, 5.6 g) in benzene (200 mL) was added dropwise a benzene (50 mL) solution of 3,4-dichloroacetophenone 5.1 (0.05 mol, 9.45 g) and diethyloxalate (0.055 mol, 8.1 g). The resultant mixture was stirred for 8 h at room temperature, then 10% aqueous HCl solution (100 mL) was added to the mixture. The organic layer was separated and washed with brine, dried over sodium sulfate and concentrated in vacuo. The crude product was purified by column chromatography using dichloromethane as eluent to yield the title compound. Yield: 7.5 g (52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871761B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-1934ae3a8e0442dda759df426fd55823 |
| Source note | uspto-grants-2014_10 |