HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → HCID 22759231, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22759269 | HCID 22759269 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22759231 | HCID 22759231 | — |
Reaction Steps
Sodium hydride (0.04 mole) is added in portions with stirring to benzyl alcohol (25 ml.). To the resulting solution, ethyl 8-acetyl-12,13-epoxytridecanoate (0.02 mole) is added and the mixture allowed to stand 18 hours at 55°-60°. The reaction mixture is then cooled and treated with water. The organic layer is separated and dried over magnesium sulfate. Excess benzyl alcohol is removed by distillation in vacuo by means of the rotary evaporator at oil pump pressure. The residue consists mainly of the title compound and is used in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04020177 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-5ad1cb0b87664dcb971bafe4154b64bc |
| Source note | uspto-grants-1977_04 |