HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → Ethyl 2-ethoxycarbonyl-9-phenoxynonanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 7-Phenoxyheptyl bromide | HCID 10516252 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-ethoxycarbonyl-9-phenoxynonanoate | HCID 18795066 | 63% |
Reaction Steps
Sodium (0.22 g, 9.6 mmol) was dissolved in EtOH (20 mL). Diethyl malonate (1.53 g, 9.6 mmol) in EtOH (5 mL) and 7-phenoxyheptyl bromide (2.36 g, 8.7 mmol) in EtOH (5 mL) were subsequently added at room temperature. The reaction mixture was refluxed for 8 h. After evaporation of the solvent, the residue was taken up in ethyl acetate (150 ml). The organic phase was washed with water (2×50 mL), and brine (50 mL), and dried over Na2SO4. The crude product was purified by Kugelrohr distillation to give ethyl 2-ethoxycarbonyl-9-phenoxynonanoate (1.92 g, 63%), bp 150-154° C./0.1 torr, 1H-NMR: 1.24 (t, 6H), 1.1-1.8 (m, 12H), 3.30 (t, 1H), 3.91 (t, 2H), 4.18 (q, 4H), 6.7-7.2 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998642 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-9d5194530c2b449796b30feeed9433fd |
| Source note | uspto-grants-1999_12 |