HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 22759289, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 22759318 | HCID 22759318 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22759289 | HCID 22759289 | — |
Reaction Steps
Lithium aluminum hydride (7.6 g., 0.2 mole) is dissolved in ether (225 ml.) and 1-(2-tetrahydropyranyloxy)-4-hydroxy-5-(4-fluorophenoxy)-2-pentyne (35.2 g., 0.12 mole) is added dropwise with stirring during 1.5 hour. The resulting mixture is stirred at 25° for 21 hours and then heated at reflux for 4 hours. The mixture is cooled and treated dropwise with ethyl acetate to consume excess lithium aluminum hydride. It is then poured into 600 ml. of ice-cold 20% aqueous potassium hydroxide solution. The oily product is taken up in ether, washed with water and brine, and dried over magnesium sulfate. Removal of solvent under vacuum leaves the title compound as a yellow residual oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061643 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-548d4428fce841fb8071c0388cfc34bf |
| Source note | uspto-grants-1977_12 |