Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | Triisopropyl borate | HCID 21531 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Edukt | 2-Fluoro-6-octyloxypyridine | HCID 19046937 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | HCID 86585711 | HCID 86585711 | — |
| Produkt | 2-Fluoro-6-octyloxypyridine-3-boronic acid | HCID 19046940 | 58,1% |
Reaktionsschritte
34.62 ml (69.24 mmol) of a 2-molar solution of lithium diisopropylamide in tetrahydrofuran/hexane/ethylbenzene are added dropwise at -78° C. to 13.00 g (57.70 mmol) of 2-fluoro-6-octyloxypyridine in 200 ml of tetrahydrofuran, and the mixture is stirred for 4 hours. 26.05 g (138.48 mmol) of triisopropyl borate are then added dropwise at -78° C., and the reaction mixture is stirred overnight, during which it warms to room temperature. After addition of 80 ml of 10% hydrochloric acid and stirring at room temperature for 1 hour, sodium chloride solution is added, the mixture is extracted with ether, the ether phase is washed with sodium chloride solution, dried over sodium sulfate, filtered and concentrated. Recrystallization from acetonitrile gives 9.03 g (33.55 mmol) of 2-fluoro-6-octyloxypyridine-3-boronic acid. ##STR22##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05630962 |
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| Quelldatensatz | uspto-grants-1997_05 |
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| ORD ID | ord-c38e4cfaab654911b6722d8cb1c59be2 |
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| Quellennotiz | uspto-grants-1997_05 |
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