Chlorotrimethylsilane → (3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenyl)trimethylsilane

Temperature

-78 °C

To a −78° C. solution of 1,4-dibromo-2-fluorobenzene (4 g, 15.75 mmol) in THF (52.5 mL) was added a solution of n-BuLi (2.5 M in hexanes; 6.3 mL, 15.75 mmol). The reaction mixture was stirred at −78° C. for 30 min 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (3.21 mL, 15.75 mmol) was then added, and the mixture was stirred at −78° C. for an additional 1 h. A solution of n-BuLi (2.5 M in hexanes; 6.3 mL, 15.75 mmol) was then added, followed after 30 min by TMSCl (4.03 mL, 31.5 mmol). The reaction mixture was allowed to warm slowly to room temperature and was stirred overnight. The mixture was then poured into a half saturated NH4Cl solution (300 mL), and the crude product was extracted with Et2O (3×). The combined organic layers were dried over MgSO4, filtered, concentrated and dried in vacuo to afford the title compound as a yellow oil (4.87 g, 11.92 mmol, 76% yield based on a 72% purity): 1H NMR (400 MHz, CDCl3) δ 7.71 (dd, J=7.2, 6.0 Hz, 1H), 7.26 (dt, J=7.2, 1.2 Hz, 1H), 7.16 (dd, J=9.6, 0.4 Hz, 1H), 1.36 (s, 12H), 0.26 (s, 9H); 19F NMR (376 MHz, CDCl3) δ −104.02; EIMS m/z 294.

1. additionwas then added
2. temperatureto warm slowly to room temperature
3. stirringwas stirred overnight
4. extractionthe crude product was extracted with Et2O (3×)
5. dry with materialThe combined organic layers were dried over MgSO4
6. filtrationfiltered
7. concentrationconcentrated
8. customdried in vacuo

ORD record

ord-eda55eae817a4277b9e7b0d68e8cbf86

Source dataset

uspto-grants-2014_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08754229B2