HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 7-oxo-7-phenylheptanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Benzoylcyclohexanone | HCID 275627 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Product | Ethyl 7-oxo-7-phenylheptanoate | HCID 11107694 | — |
Reaction Steps
A mixture of 2-benzoylcyclohexanone (1.00 g), sodium ethoxide (404 mg) in ethanol (5 mL) was stirred for 3.5 hours at room temperature. The reaction was quenched by adding 1N hydrochloric acid (1 mL). The solvent was evaporated off, and the residue was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated to give ethyl 7-oxo-7-phenylheptanoate as a brown oil (1.33 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153854B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-c27831a485234b90b51bf50b96a7b44c |
| Source note | uspto-grants-2006_12 |