Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Oxygen | HCID 977 | — |
| Edukt | Thianthrene | HCID 7109 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Edukt | HCID 178461630 | HCID 178461630 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Thianthren-1-ol | HCID 21569430 | 36% |
Reaktionsschritte
To a cooled (−78° C.) solution of thianthrene (10 g, 46.23 mmol) in anhydrous THF (200 ml) was added t-BuLi (1.7M in pentane, 40.81 ml, 69.34 mmol), under a nitrogen atmosphere, over a period of 10 minutes and the resulting yellow solution was then allowed to warm to room temperature and stirred vigorously for a further 16 hours. EtMgBr (3M in THF, 23 ml, 69.34 mmol) was then added in a dropwise fashion to the cooled (0° C.) reaction mixture which was then stirred for a further 45 minutes before oxygen was bubbled through the solution. After two hours the reaction was quenched by dropwise addition of 1M NaOH (100 ml) and washed with EtOAc (1×300 ml) before being acidified to pH4 with aqueous 1M HCl. The mixture was then extracted with EtOAc (3×100 mL),dried (MgSO4), filtered and concentrated in vacuo to give a mild amber slurry that was purified by flash chromatography (SiO2) (10:1, Ethyl acetate/Hexanes), to give the title compound (3.82 g, 36%) as a yellow solid. m/z (LC-MS, ESP):, RT=4.62 min, (M++1)=231
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07429660B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-76a248e004c4433f8e5b089409fa7051 |
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| Quellennotiz | uspto-grants-2008_09 |
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