Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylamine | HCID 7912 | — |
| Edukt | Hexachloroacetone | HCID 8303 | — |
| Edukt | 1-Bromo-2,4-difluorobenzene | HCID 67674 | — |
| Lösungsmittel | Butyllithium | HCID 178418339 | — |
| Produkt | 1-Bromo-3-chloro-2,4-difluorobenzene | HCID 2773256 | — |
Reaktionsschritte
To a solution of 19 ml (0.135 mole) of diisopropylarnine in 125 ml of tetrahydroflran (TBF) cooled at −20° C. is added 80 ml of n-butyllithium (1.6 M in hexane). The temperature is raised to 0° C. for 5 minutes and lowered to −78° C. Then 25 g (0.129 mole) of 2,4-difluoro-bromobenzene is then added and the reaction is stirred at −65° C. for 2 hours. Then, 25 ml (0.164 mole) of hexachloroacetone is added and the solution is warmed at room temperature. After evaporation of the solvent, the residue is distilled under vacuum to give the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06348624B1 |
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| Quelldatensatz | uspto-grants-2002_02 |
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| ORD ID | ord-8c047c2ef56049ac90d663ea63b103bc |
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| Quellennotiz | uspto-grants-2002_02 |
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