HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methylfuran → (1R*,5S*)-2,3,4,4-tetrachloro-1-methyl-8-oxabicyclo[3.2.1]octa-2,6-diene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methylfuran | HCID 10797 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Pentachlorocyclopropane | HCID 22631 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Product | (1R*,5S*)-2,3,4,4-tetrachloro-1-methyl-8-oxabicyclo[3.2.1]octa-2,6-diene | HCID 67533581 | — |
Reaction Steps
Pentachlorocyclopropane (100 g, 0.467 mol) is added to a suspension of potassium hydroxide (31.4 g, 0.56 mol) in 1,4-dioxane (3600 ml) and the mixture is stirred at room temperature for 30 minutes and then heated to 65° C. for a further 30 minutes. 2-Methylfuran (38.36 g, 0.467 mol) is added to the reaction mixture, the temperature is raised to 85-90° C. and the mixture is stirred for 16 hours. The reaction mixture is cooled to room temperature, filtered through a plug of diatomaceous earth and the filtrate evaporated in vacuo to give (1R*,5S*)-2,3,4,4-tetrachloro-1-methyl-8-oxabicyclo[3.2.1]octa-2,6-diene (83 g), used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006429B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-bc3e11c4f9b8412dbfaf95f5e55bbadf |
| Source note | uspto-grants-2015_04 |