HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-dihydro-2H-pyran → 3-Methyl-4-(tetrahydropyran-2-yloxy)-1-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | 2-Methyl-3-buten-1-ol | HCID 94292 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Methyl-4-(tetrahydropyran-2-yloxy)-1-butene | HCID 15625011 | 75.3% |
Reaction Steps
A solution of 2-methyl-3-buten-1-ol (54.16 g, 0.63 m), dihydropyran (52.92 g, 0.63 m), and p-toluenesulfonic acid (0.5 g) in ether (800 ml) is stirred at room temperature under a nitrogen atmosphere overnight. The reaction mixture is then diluted with ether (1 l) and washed with 5% sodium bicarbonate solution (1 l). The ether extract is dried (Na2SO4), filtered and solvent removed in vacuo to give 95.8 g of crude product. The crude product is purified by column chromatography on silica gel (500 g, hexane) to give (75%) 3-methyl-4-(tetrahydropyran-2-yloxy)-1-butene (80.62 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04237054 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-a473fbe9568f4ca0b4560298792d3d7d |
| Source note | uspto-grants-1980_12 |