Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2-Bromobiphenyl | HCID 16329 | — |
| Edukt | 3-Phenylphthalide | HCID 95365 | — |
| Edukt | HCID 178418244 | HCID 178418244 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 59642515 | HCID 59642515 | — |
Reaktionsschritte
In Ar, 3.9 g (1.68E-2 mol) of o-bromobiphenyl was dissolved in 30 cm3 of tetrahydrofuran (THF) at −50° C. To the solution was added 10 cM3 of a nBuLi hexane solution (1.5 mol/l). After 2 hours, 3 g (1.4E-2 mol) of 3-phenylphthalide was added to the solution while it was kept cooled at −50° C. After 2 hours, the reaction solution was allowed to resume room temperature, and 10 cm3 of a 35% aqueous hydrochloric acid was added thereto. After 1 hour, toluene extraction was carried out using a separatory funnel, followed by thorough washing with distilled water. After the toluene solution was concentrated, the end product was isolated by silica gel chromatography (developer, toluene:hexane=1:4). There was obtained 4 g (80%) of a yellow viscous substance emitting bluish green fluorescence.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07732652B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-aff8c3652e3f40dfb2b6af6c85dd89ca |
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| Quellennotiz | uspto-grants-2010_06 |
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