HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl benzoylacetate → HCID 20200616, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl benzoylacetate | HCID 7170 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 1-(Chloromethyl)-2-(3-chloropropyl)benzene | HCID 12373990 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20200616 | HCID 20200616 | — |
Reaction Steps
A stirred solution of sodium ethoxide (from 0.53 g. sodium) in ethanol (80 ml.) was treated with ethyl benzoylacetate (4.42 g.). After 1 hour, -(o-chloromethylphenyl)propyl chloride (4.57 g.) was added and stirring was continued for 24 hours. The mixture was then diluted with ether (100 ml.) and water (100 ml.). The organic layer was separated, washed with saturated brine (50 ml.), dried (MgSO4) and evaporated to give ethyl 2-benzoyl-3-(o-(3-chloropropyl)phenyl]propanoate (A) as a yellow oil (7.66 g.), NMR: 1.1 (3H,t), 2.1 (2H,m), 2.7-3.7 (6H,m), 4.1 (2H,m), 4.65 (1H,t) and 7.0-8.2 (9H,m)ppm, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04668698 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-243576552d244c86b7b48fc100e7caff |
| Source note | uspto-grants-1987_05 |