HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-dihydro-2H-pyran → 1-Acetoxy-8-(2-tetrahydropyranyl)oxy-3,7-dimethyl-2,6-octadiene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 8-Acetoxy-2,6-dimethyl-2,6-octadien-1-ol | HCID 53904329 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Acetoxy-8-(2-tetrahydropyranyl)oxy-3,7-dimethyl-2,6-octadiene | HCID 53657563 | 96% |
Reaction Steps
A mixture of 8-acetoxy-2,6-dimethyl-2,6-octadiene-1-ol (1.81 g, 8.52 mmol) and dihydropyran (1.17 ml, 12.8 mmol) in dichloromethane (6 ml) was stirred, and p-toluenesulfonic acid (40 mg) was added thereto, and the mixture was stirred at room temperature for 30 minutes. After addition of saturated aqueous sodium bicarbonate (30 ml), the product was extracted with hexane/ether (5:1.1) (30 ml). The extract was dried over Na2SO4 and evaporated in vacuo to remove the solvent to give a residue, which was purified with silica gel column chromatography to give 1-acetoxy-8-(2-tetrahydropyranyl)oxy-3,7-dimethyl-2,6-octadiene (2.42 g, 96%). ##STR58##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05324869 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-2e593b20c41144edac361aa9f574076e |
| Source note | uspto-grants-1994_06 |