HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl (2-chlorobenzoyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethanone, 1-(2-chlorophenyl)- | HCID 72864 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl (2-chlorobenzoyl)acetate | HCID 292405 | — |
Reaction Steps
Sodium hydride (8.7 grams) and 21.4 grams of diethyl carbonate are suspended in 100 ml of tetrahydrofuran, 14 grams of o-chloroacetophenone is gradually dropped thereinto by keeping the inner temperature at 40° to 50° C., then a small amount of ethanol is added thereto and heated to reflux for four hours. After cooling, 20 ml of ethanol is added thereto, the mixture is poured into ice water, and extracted with ether. Ether extracts are combined, washed with water, dried with anhydrous magnesium sulfate, and ether is evaporated therefrom. The resulting oil is purified by distillation in vacuo to give 8.8 grams of colorless, oily product, b.p. 120° to 125° C./1 mmg Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04711898 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-3823c647e0a742aa85112ba7366a48a0 |
| Source note | uspto-grants-1987_12 |