HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3,5-Trioxane → 6,7-dihydro-4H-thieno[3,2-c]pyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3,5-Trioxane | HCID 8081 | — |
| Reactant | 2-Thiopheneethanol | HCID 79400 | — |
| Catalyst | indium(III)chloride | HCID 159675 | — |
| Solvent | Butyronitrile | HCID 8008 | — |
| Product | 6,7-dihydro-4H-thieno[3,2-c]pyran | HCID 11469118 | 121.2% |
Reaction Steps
10.0 g of 2-thiopheneethanol, 3.5 g of 1,3,5-trioxane, and 862 mg of indium(III) chloride were added to 1,500 mL of butyronitrile, and the resulting mixture was refluxed for 6 hours. The reaction product solution was cooled to room temperature and concentrated by evaporation under reduced pressure. The residue was distilled under reduced pressure to obtain 6.6 g (yield of 60%) of the title compound, of which analysis data were the same as obtained in Example 14.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07449580B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-efa264e3dca74563bf547189cf36dec9 |
| Source note | uspto-grants-2008_11 |