Reaktion #2371656
ord-a6b9e96d0f824dee815dc3c2927473e0
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeReaction mixture
- 2workup.ADDITIONwas then treated
- 3workup.ADDITIONwas added via syringe
- 4Temperaturthe reaction mixture was warmed to room temperature
- 5Sonstigebefore quenching
- 6Sonstigethe reaction with equal volume of concentrated NH4Cl(aq) and EtOAc (1:1, 30 mL)
- 7SonstigeThe layers were separated
- 8Extraktionthe water phase was further extracted with equal volume of EtOAc before the organic layers
- 9Trocknendried over anhydrous Na2SO4
- 10Filtrationfiltered
- 11SonstigeThe solvent was removed under reduced pressure
- 12SonstigeThe residue was purified by silica gel column
Vorschrift
A solution of 2-(4-bromo-2-fluoro-5-((tetrahydro-2H-pyran-2-yloxy)methyl)phenoxy)tetrahydro-2H-pyran (6.31 g, 16.2 mmol) in anhydrous THF (13.5 mL) was made before cooling the reaction mixture in a −78° C. bath. Reaction mixture was then treated, drop-wise, with n-BuLi (12.15 mL, 19.45 mmol) and allowed to stir for 1.0 hr before (i-PrO)3B (5.59 mL, 24.3 mmol) was added via syringe. After the addition of (i-PrO)3B, the reaction mixture was warmed to room temperature and allowed to stir for 2 hr before quenching the reaction with equal volume of concentrated NH4Cl(aq) and EtOAc (1:1, 30 mL). The layers were separated and the water phase was further extracted with equal volume of EtOAc before the organic layers were combined and dried over anhydrous Na2SO4 and filtered. The solvent was removed under reduced pressure. The residue was purified by silica gel column using Combiflash to give 6-fluorobenzo[c][1,2]oxaborole-1,5(3H)-diol (2.01 g, 73.93%). 1H-NMR (400 MHz, DMSO-d6) δ (ppm) 4.85 (s, 2H), 6.95 (d, J=5.4 Hz, 1H), 7.36 (d, J=8.1 Hz, 1H), 8.98 (s, 1H), 10.22 (s, 1H).