HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Butyne-1,4-diol → 4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Butyne-1,4-diol | HCID 8066 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol | HCID 11123315 | 68.8% |
Reaction Steps
To a mixture of 5.0 g of 2-butyne-l,4-diol and 10 milligrams of p-toluenesulfonic acid and 150 ml of dry ether there was added dropwise with stirring at room temperature 4.9 g of 3,4-dihydro-2H-pyran. After stirring overnight at ambient temperature the ether was evaporated and the residue was poured into 200 ml of water. The aqueous solution was extracted with hexane (2×100 ml) and then re-extracted with ether (3×100 ml). The combined ether extracts were washed with 100 ml of brine, dried over magnesium sulfate and evaporated to yield 6.8 g of 4-tetrahydropyranoxy-2-butyn-1-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05728694 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-b5f509f406ce44cc9d59d96a369153b8 |
| Source note | uspto-grants-1998_03 |