HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl alcohol → Tetrahydro-2-(2-propynyloxy)-2H-pyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Product | Tetrahydro-2-(2-propynyloxy)-2H-pyran | HCID 98609 | 95% |
Reaction Steps
Propargyl alcohol (13.20 g) and dihydropyran (19.81 g) are placed into a 50-ml container, and 0.2 g of anhydrous p-toluenesulfonic acid is added. The mixture is cooled in an ice bath, then stirred at room temperature for 30 minutes and neutralized with anhydrous sodium carbonate. The resulting solids are separated off. Distillation of the remaining liquid in a vacuum gives 31.3 g of propargyl tetrahydropyranyl ether (yield: 95%), b.p. 75° to 80° C./37 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04186141 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-241dbcadfc6646149c7014b6a3e1a3fb |
| Source note | uspto-grants-1980_01 |