Hydrochloric Acid → 3-{[Tert-butyl(dimethyl)silyl]oxy}-2-fluorobenzaldehyde

Sec-BuLi (1.3M solution in cyclohexane, 75 mL, 98 mmol) was added slowly at −78° C. to a solution of Intermediate 31, 1-(tert-Butyldimethylsilyl)oxy-2-fluorobenzene (20.1 g, 89 mmol) and TMEDA (14.8 mL, 98 mmol) in THF (200 mL) and the mixture was stirred at the same temperature for 30 min. DMF (7.5 mL, 98 mmol) was added to the mixture at −78° C., and the mixture was stirred at the same temperature for 1.5 h. Then 10% aqueous HCl was added to attain pH˜4-5 (200 mL), and the reaction mixture was stirred at RT for 30 min. The organic layer was separated. Aqueous layer was extracted with EtOAc (200 mL). The organic layers was washed with sat. NaHCO3, brine, dried with Na2SO4 and evaporated in vacuo to give the title compound (16.7 g, 74%, 66 mmol) as a yellow oil. 1H NMR data (dmso-d6): 10.21 (s, 1H, CHO), 7.39-7.45 (m, 1H, H—Ar), 7.32-7.38 (m, 1H, H—Ar), 7.22-7.28 (m, 1H, H—Ar), 0.97 (s, 9H, t-Bu), 0.20 (s, 6H, 2CH3).

1. stirringthe mixture was stirred at the same temperature for 1.5 h
2. stirringthe reaction mixture was stirred at RT for 30 min
3. customThe organic layer was separated
4. extractionAqueous layer was extracted with EtOAc (200 mL)
5. washThe organic layers was washed with sat. NaHCO3, brine
6. dry with materialdried with Na2SO4
7. customevaporated in vacuo

ORD record

ord-5296f5849c8c4bf3bdfbf6c60a666fdf

Source dataset

uspto-grants-2010_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07812040B2