Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Phenyl-1-pentanol | HCID 61523 | — |
| Reactant | propiolic acid, sodium salt | HCID 4314123 | — |
| Reactant | 2-Propynoyl chloride | HCID 12260668 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Propynoyl chloride | HCID 12260668 | — |
| Product | 5-Phenylpentyl propiolate | HCID 18981481 | — |
Reaction Steps
With stirring, 1 gram of 5-phenylpentanol was added dropwise to a mixture of 0.25 g of sodium hydride (60% oil suspension) and 25 ml of dried benzene. The mixed solution is further stirred at ambient temperatures for one hour. A benzene solution of propiolic acid chloride is prepared by stirring a mixture of 0.62 g of sodium propiolate, 0.80 g of thionyl chloride, and 20 ml of dried benzene at ambient temperatures for five hours. The benzene solution of propiolic acid chloride thus prepared is added to the mixed solution, stirred at ambient temperatures for five hours, and refluxed for one hour. After the reaction is completed, the reaction solution is washed successively with water and a saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. After removal of the solvent under reduced pressure, the obtained residue is subjected to silicagel column chromatography to yield 5-phenylpentyl propiolate (compound 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05502242 |
|---|
| Source dataset | uspto-grants-1996_03 |
|---|
| ORD ID | ord-1c3d68f2142e4ab181486f06fd3e2a66 |
|---|
| Source note | uspto-grants-1996_03 |
|---|