HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Ethyl 8-(2-chloroethylthio)-12-acetoxyheptadecanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21317600 | HCID 21317600 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 8-(2-chloroethylthio)-12-acetoxyheptadecanoate | HCID 21317532 | — |
Reaction Steps
Thionyl chloride (13.1 g., 0.11 mole) is added dropwise with stirring to a solution of ethyl 8-(2-hydroxyethylthio)-12-acetoxyheptadecanoate (43.2 g., 0.10 mole) in benzene (150 ml.). The solution is heated at reflux for 2 hours. Then, the solvent and excess thionyl chloride are removed by evaporation in vacuo to leave the title compound as an orange yellow residual oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04018802 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-de56ea68853742879cd6376df4bf57e9 |
| Source note | uspto-grants-1977_04 |