HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl iodide → 1-Ethyl hydrogen 4-oxo-4H-quinolizine-1,3-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | Diethyl 4-oxo-4H-quinolizine-1,3-dicarboxylate | HCID 262620 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-Ethyl hydrogen 4-oxo-4H-quinolizine-1,3-dicarboxylate | HCID 621509 | 87.9% |
Reaction Steps
To a solution of 1,3-diethoxycarbonyl-4H-quinolizin-4-one (1 g) in chloroform (20 ml) was added trimethylsilyl iodide (0.49 ml) at room temperature and the mixture was stirred for 4 hours and heated with reflux for 4 hours. After cooling to room temperature, the mixture was washed with water, aqueous sodium thiosulfate, and brine. Drying over magnesium sulfate and evaporation gave a crystalline residue, which was washed with isopropyl alcohol to give 1-ethoxycarbonyl4H-quinolizin-4-one-3-carboxylic acid (794 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04698349 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-8ca7f7cbfe3a459bbc405f84de8111ee |
| Source note | uspto-grants-1987_10 |