HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Ethyl 2-methyl-5-(2-phenylethyl)-1,3-oxazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21417731 | HCID 21417731 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-methyl-5-(2-phenylethyl)-1,3-oxazole-4-carboxylate | HCID 21417734 | — |
Reaction Steps
To the entire oily residue obtained in Step A is added at 0° C., 60 ml. of thionyl chloride and the resulting mixture refluxed for 40 minutes. The reaction mixture is then cooled and evaporated (under vacuum) to obtain a residue. The residue is dissolved in methylene chloride, and the solution washed with 5% aqueous sodium bicarbonate (100 ml.). The organic layer is then dried over anhydrous sodium sulfate and evaporated (under vacuum) to obtain the title compound as a crude residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04042596 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-babd5c12c6cb4fdbb5ec5fcfdfdfe03c |
| Source note | uspto-grants-1977_08 |