HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromofuran → (1RS, 2RS,6SR,7SR)-8-bromo-4-(2,4,6-trimethylphenyl)-10-oxatricyclo-[5.2.1.02,6]dec-8-en-3,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromofuran | HCID 89164 | — |
| Reactant | Magnesium diiodide | HCID 5462737 | — |
| Reactant | 2-(2,4,6-Trimethylphenyl)cyclopent-4-ene-1,3-dione | HCID 66684424 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1RS, 2RS,6SR,7SR)-8-bromo-4-(2,4,6-trimethylphenyl)-10-oxatricyclo-[5.2.1.02,6]dec-8-en-3,5-dione | HCID 67284125 | — |
Reaction Steps
3-Bromofuran (5.2 g, 56 mmol) and magnesium iodide (1.5 g, 5.6 mmol) are added to 2-(2,4,6-trimethylphenyl)cyclopent-4-ene-1,3-dione (4.0 g, 18.7 mmol) and the mixture is stirred at room temperature for 2 days; small quantities of dichloromethane are added when required to aid stirring. The reaction mixture is allowed to stand at room temperature for 17 hours, then concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to give (1RS, 2RS,6SR,7SR)-8-bromo-4-(2,4,6-trimethylphenyl)-10-oxatricyclo-[5.2.1.02,6]dec-8-en-3,5-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754242B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-3f6249c8f1ef4ca0ad83b3146435265c |
| Source note | uspto-grants-2014_06 |