Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Decalin | HCID 7044 | — |
| Edukt | Dibenz(b,f)azepine | HCID 9212 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 4,4'-Diiodo-1,1'-biphenyl | HCID 76348 | — |
| Katalysator | Copper | HCID 23978 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 5-(4'-Iodobiphenyl-4-yl)dibenz[b,f]azepine | HCID 21311077 | 50% |
Reaktionsschritte
5H-Dibenz[b,f]azepine in an amount of 20.0 g (0.10 mol), 4,4'-diiodobiphenyl in an amount of 60.9 g (0.15 mol), potassium hydroxide in an amount of 6.7 g (0.12 mol) and a copper powder in an amount of 1.3 g (0.02 mol) were mixed with 20 ml of decalin, and heated with stirring in a stream of nitrogen for 36 hours at the external temperature of 200° C. After cooling to room temperature or its vicinity, the reaction solution was admixed with chloroform, and subjected to Celite filtration to remove the insoluble matter. The filtrate was concentrated, and the concentrated solution was purified by column chromatography on silica gel. Thus, 23.6 g of 5-(4'-iodobiphenyl-4-yl)dibenz[b,f]azepine was obtained (in a 50% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05929235 |
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| Quelldatensatz | uspto-grants-1999_07 |
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| ORD ID | ord-92c8721821554ee5abeb0f6e915bc73b |
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| Quellennotiz | uspto-grants-1999_07 |
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