Reaktion #1938311
ord-9346972a12ce4818a2eec53723aff655
Reaktionsgleichung
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigesealed with a rubber septum
- 2Sonstigethe mixture was degassed 10 min
- 3Sonstigeby sparging with N2
- 4Sonstigewhile immersed in an ultrasonic bath
- 5Temperaturthe mixture was cooled
- 6Filtrationfiltered through a pad of Celite
- 7WaschenThe filtrate was washed (satd NH4Cl×2, water, brine)
- 8Trocknendried over Na2SO4
- 9Einengenconcentrated in vacuo
- 10SonstigeThe residue was purified by low pressure liquid chromatography (silica gel, EtOAc/hexanes, gradient elution)
Vorschrift
A thick-walled glass vessel was charged with 1,2-dibromo-4-fluoro-3-iodobenzene (8.31 g, 21.88 mmol), Pd(PPh3)2Cl2 (0.768 g, 1.094 mmol), and CuI (0.292 g, 1.532 mmol) and sealed with a rubber septum. Anhyd THF (30 mL) and DIPA (30.8 mL, 219 mmol) were added via syringe and the mixture was degassed 10 min by sparging with N2 while immersed in an ultrasonic bath. Ethynyltrimethylsilane (3.40 mL, 24.07 mmol) was added via syringe and the septum was replaced with a PTFE bushing. The mixture was stirred in an oil bath at 40° C. After 40 h, the mixture was cooled, diluted with EtOAc and filtered through a pad of Celite. The filtrate was washed (satd NH4Cl×2, water, brine), dried over Na2SO4 and concentrated in vacuo. The residue was purified by low pressure liquid chromatography (silica gel, EtOAc/hexanes, gradient elution) affording ((2,3-dibromo-6-fluorophenyl)ethynyl)trimethylsilane (6.08 g, 17.37 mmol, 79% yield) as a yellow oil: 1H NMR (400 MHz, CDCl3) δ 7.53 (dd, J=8.9, 5.4 Hz, 1H), 6.95 (dd, J=8.9, 8.1 Hz, 1H), 0.29 (s, 9H); MS (GCMS EI) m/z 348 ([M]+, Br isotopes, 18%), 350 ([M]+, Br isotopes, 34%), 352 ([M]+, Br isotopes, 18%), 333 ([M-CH3]+, Br isotopes, 56%), 335 ([M-CH3]+, Br isotopes, 100%), 337 ([M-CH3]+, Br isotopes, 54%).