Tetrahydrofuran → 3-Bromo-2,4-difluorobenzaldehyde

To a cooled (0° C.) solution of 2,2,6,6-tetramethylpiperidine (1.64 mL, 9.75 mmol) in THF (20 mL) was added 1.6 M n-butyllithium in hexane (5.54 mL, 8.86 mmol). The solution was stirred for 20 min, then brought to −78° C. 1-bromo-2,6-difluorobenzene (1.00 mL, 8.86 mmol) in THF was added slowly, and the solution was stirred at −78° C. for 30 min. DMF (1 mL) was added slowly, and the solution was stirred at −78° C. for 20 min. Saturated aqueous ammonium chloride was added and the reaction was allowed to warm to rt. The organic solvent was removed in vacuo, and the residual material was extracted with EtOAc and washed with water (2×). The organic layer was purified by column chromatography (1 to 2% EtOAc:hexanes) to afford 350 mg (18%) of the title compound as a yellow solid. 1H NMR (400 MHz, CDCl3): δ 6.97 (td, J=9.2, 1.5 Hz, 1 H), 7.78 (ddd, J=9.0, 7.5, 5.7 Hz, 1 H), 10.34 (s, 1 H).

1. custombrought to −78° C
2. stirringthe solution was stirred at −78° C. for 30 min
3. stirringthe solution was stirred at −78° C. for 20 min
4. customThe organic solvent was removed in vacuo
5. extractionthe residual material was extracted with EtOAc
6. washwashed with water (2×)
7. customThe organic layer was purified by column chromatography (1 to 2% EtOAc:hexanes)

ORD record

ord-2540c8277cd7462886c0a3f04debfd59

Source dataset

uspto-grants-2013_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08378104B2