HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5-phenyl-4-pentyn-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-[(5-Phenylpent-4-yn-1-yl)oxy]oxane | HCID 53944465 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-phenyl-4-pentyn-1-ol | HCID 11137434 | — |
Reaction Steps
A mixture of 1-phenyl-5-tetrahydropyranyloxypent-1-yne (0.2 g), absolute ethanol (4 ml) and p-toluenesulphonic acid (20 mg) was stirred at room temperature for 3 hours. The reaction mixture was diluted with water (40 ml) and extracted with ether (2×20 ml). The ether extracts were washed with saturated NaHCO3 solution, dried over MgSO4 and purified by chromatography on silica (20 g), eluting with 10% ether in hexane grading to 100% ether, followed by 10% ether acetate in ether. The solvent was removed to give 5-phenylpent-4-yn-1-ol as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855086 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-6df700751b734b82a680b0fda4d41af5 |
| Source note | uspto-grants-1989_08 |