Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 59497131 | HCID 59497131 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59497125 | HCID 59497125 | 27% |
Reaction Steps
A solution of SeO2 (0.98 g, 8.8 mmol) in a mixture of dioxane (50 mL) and water (2 mL) was heated to reflux in a two-neck 250 mL round-bottomed flask. A solution of 2-methyl-4-propylsulfanyl-[1,10]phenanthroline (0.95 g, 3.5 mmol) in hot dioxane (50 mL) was added through an addition funnel over a period of 30 minutes and the reaction mixture was refluxed for additional 1 hour. The reaction mixture was filtered while hot and the residue rinsed with more hot dioxane (20 mL) and filtered. The filtrates were combined and evaporated in vacuo and the residue was treated with methylene chloride (100 mL) and a 10% K2CO3 aqueous solution (100 mL). The aqueous layer was extracted several times with methylene chloride (3×100 mL) and the combined organic layers were washed with brine, dried (Na2SO4), filtered and concentrated. The crude product was purified by flash chromatography (neutral Al2O3, MeOH/DCM, 1:50 to 1:15) to afford the pure product as a brown solid (0.27 g, 27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592446B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-7a26163ff3494652b55d32d9fbe06aeb |
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| Source note | uspto-grants-2013_11 |
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